CAS: 942-92-7; Hexanophenone

该化合物是属于氯酮类的有机化合物,其特征为附于苯乙烯功能组的六碳烷基链(赫克松),该元素组由碳基(C=O)组成,联苯环系.该元素既具有对分子的疏水性和对脂性,又具有对分子的亲脂性,使其在有机溶剂中溶解,但在水中较少.乙诺芬作为色素一般出现在具有独特气味的浅色黄色液体中.它用于各种用途,包括溶剂,香味合成和有机合成的中间.该化合物可能具有中度毒性,在处理时应当采取适当的安全措施.其物理特性,如沸点和熔点,可以因纯度和环境条件而不同而不同.它与许多金酮一样,可能参与典型的碳基化合物反应,包括核糖添加和氧化.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

pyridine bis-(1-phenyl-cyclohexyl)-peroxide 1-bromo-butane α-methoxystyrene2-hydroxy-2-phenyl-heptanoic acid amide 2-phenylheptane-2-ol 1-phenyl-2-piperidinomethyl-hexan-1-one; hydr°Chloride (E)-1-phenyl-1,2-hexanedione 2-oxime

合成工艺路线路线简述

  • 合成目标产物 Hexanophenone 主要起始原料 Hexanoyl Chloride And Benzene
  • 1804967-87-0 + 308796-10-3 = 942-92-7
    反应条件:1.1 Catalysts: Cobalt Dibromide Solvents: Tetrahydrofuran,1,4-Dioxane; Overnight,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Rt
    标题:Cobalt Bromide-Catalyzed Negishi-Type Cross-Coupling Of Amides
    作者:Dorval,Celine; Stetsiuk,Oleh; Gaillard,Sylvaine; Dubois,Elodie; Gosmini,Corinne; Et Al
    参考文献:Organic Letters 日期:2022 卷标:24(14) 页码:2778-2782]

    98-80-6 + 2051-49-2 = 942-92-7
    反应条件:1.1 Reagents: Water Catalysts: Triphenylphosphine,Palladium Diacetate Solvents: Tetrahydrofuran
    标题:Preparation Of Ketones From Carboxylic Acid Anhydrides And Boronic Acids
    参考文献:World Intellectual Property Organization]

    4471-05-0 = 942-92-7
    反应条件:1.1 Catalysts: Ethyl 2-Mercaptopropionate,2,4,5,6-Tetra(9H-Carbazol-9-Yl)Isophthalonitrile Solvents: Ethyl Acetate; 3 H,Rt
    标题:Photochemical Hydrogen Atom Transfer Catalysis For Dehydrogenation Of Alcohols To Form Carbonyls
    作者:Yang,Xiaona; Guo,Yunfei; Tong,Hong'En; Guo,Hongyu; Liu,Rongfang; Et Al
    参考文献:Organic Letters 日期:2023 卷标:25(29) 页码:5486-5491]

    209069-35-2 = 942-92-7
    反应条件:1.1 Catalysts: Di-μ-Chlorobis[(1,2,5,6-η)-1,3,5,7-Cyclooctatetraene]Dirhodium,1,1′-(9,9-Dimethyl-9H-Xanthene-4,5-Diyl)Bis[1,1-Diphenylphosphine] Solvents: Tetrahydrofuran; 10 Min,Rt1.2 Catalysts: Cesium Acetate; 10 Min,Rt1.3 Solvents: Tetrahydrofuran; 15 H,70 °C
    标题:Rhodium-Catalyzed Remote Isomerization Of Alkenyl Alcohols To Ketones
    作者:Dong,Wenke; Yang,Hongxuan; Yang,Wen; Zhao,Wanxiang
    参考文献:Organic Letters 日期:2020 卷标:22(4) 页码:1265-1269]

    98-80-6 + 2051-49-2 = 942-92-7
    反应条件:1.1 Catalysts: Palladium Diacetate,Tris(2-Methoxyphenyl)Phosphine Solvents: Tetrahydrofuran,Water; 16 H,60 °C1.2 Solvents: Dichloromethane
    标题:Palladium-Catalyzed Synthesis Of Aryl Ketones From Boronic Acids And Carboxylic Acids Activated In Situ By Pivalic Anhydride
    作者:Goossen,Lukas J.; Ghosh,Keya
    参考文献:European Journal Of Organic Chemistry 日期:2002 卷标:(19) 页码:3254-3267]

    591-51-5 = 942-92-7
    反应条件:1.1 Reagents: Morpholine,Diisobutylaluminum Hydride Solvents: Tetrahydrofuran,Hexane; 0 °C; 3 H,0 °C1.2 0 °C; 10 Min,0 °C1.3 Solvents: Hexane; 30 Min,0 °C1.4 Reagents: Hydrochloric Acid Solvents: Water; 0 °C
    标题:An Effective One-Pot Conversion Of Acid Chlorides To Aldehydes And Ketones
    作者:Park,Jae Kyo; Shin,Won Kyu; An,Duk Keun
    参考文献:Tetrahedron Letters 日期:2013 卷标:54(24) 页码:3199-3203]

    627-27-0 = 942-92-7
    反应条件:1.1 Reagents: Cesium Carbonate Catalysts: Iridium,Aqua[[2,2′-Bipyridine]-6,6′(1H,1′h)-Dionato(2-)-Kn1,Kn1′][(1,2,3,4,5-η)... Solvents: 2-Methyl-2-Butanol; 12 H,125 °C
    标题:Direct Couplings Of Secondary Alcohols With Primary Alkenyl Alcohols To α-Alkylated Ketones Via A Tandem Transfer Hydrogenation/hydrogen Autotransfer Process Catalyzed By A Metal-Ligand Bifunctional Iridium Catalyst
    作者:Xu,Xiangchao; Li,Shun; Luo,Shiyuan; Yang,Jiazhi; Li,Feng
    参考文献:Journal Of Catalysis 日期:2022 卷标:413 页码:365-373]

    98-80-6 + 7391-39-1 = 942-92-7
    反应条件:1.1 Reagents: Oxygen Catalysts: Palladium Diacetate,2-(3,5-Dimethyl-1H-Pyrazol-1-Yl)Pyridine Solvents: 1,2-Dimethoxyethane,Trifluoromethanesulfonic Acid,Water; 12 H,60 °C1.2 Reagents: Sodium Bicarbonate Solvents: Water; Neutralized
    标题:Palladium Catalyzed Decarboxylative Acylation Of Arylboronic Acid With Ethyl Cyanoacetate As A New Acylating Agent: Synthesis Of Alkyl Aryl Ketones
    作者:Yousuf,Md; Das,Tuluma; Adhikari,Susanta
    参考文献:New Journal Of Chemistry 日期:2015 卷标:39(11) 页码:8763-8770]

    1129-65-3 = 942-92-7
    反应条件:1.1 Catalysts: Iron Chloride (Fecl3),[1,1,1-Trifluoro-N-[(Trifluoromethyl)Sulfonyl-Ko]Methanesulfonamidato-Ko]Silver Solvents: 1,4-Dioxane; 30 Min,Rt1.2 Reagents: Water; Rt; 60 H,95 °C
    标题:Regioselective Hydration Of Alkynes By Iron(Iii) Lewis/bronsted Catalysis
    作者:Cabrero-Antonino,Jose R.; Leyva-Perez,Antonio; Corma,Avelino
    参考文献:Chemistry - A European Journal 日期:2012 卷标:18(35) 页码:11107-11114]

    98-86-2 + 71-36-3 = 942-92-7
    反应条件:1.1 Catalysts: Cesium Carbonate,(Oc-6-42)-Bromodicarbonyl[n,N′-(6-Phenyl-1,3,5-Triazine-2,4-Diyl-Kn3)Bis[p,P-Bis... Solvents: 2-Methyl-2-Butanol; 24 H,140 °C
    标题:Manganese(I)-Catalyzed Cross-Coupling Of Ketones And Secondary Alcohols With Primary Alcohols
    作者:Gawali,Suhas Shahaji; Pandia,Biplab Keshari; Pal,Souvik; Gunanathan,Chidambaram
    参考文献:Acs Omega 日期:2019 卷标:4(6) 页码:10741-10754]

    98-80-6 + 2051-49-2 = 942-92-7
    反应条件:1.1 Reagents: Water Catalysts: Tris(4-Methoxyphenyl)Phosphine,Palladium Diacetate Solvents: Tetrahydrofuran
    标题:Palladium-Catalyzed Synthesis Of Aryl Ketones From Boronic Acids And Carboxylic Acids Or Anhydrides
    作者:Goossen,Lukas J.; Ghosh,K.
    参考文献:Angewandte Chemie 日期:2001 卷标:40(18) 页码:3458-3460]

    = 942-92-7
    反应条件:1.1 Reagents: Aluminum Chloride Solvents: Dichloromethane; 30 Min,0 °C; 30 Min,0 °C1.2 Solvents: Dichloromethane; 0 °C; 0 °C -> Rt; 1 H,Rt1.3 Reagents: Water; 0 °C
    标题:Cathinone Derivatives,Pharmaceutical Formulations,And Methods
    参考文献:United States]

    = 942-92-7
    反应条件:1.1 Catalysts: Gallium Nitride Solvents: Heptane; 4 H,90 °C
    标题:Facile Synthesis Of Crystalline Nanoporous Gan Templated By Nitrogen Enriched Mesoporous Carbon Nitride For Friedel-Crafts Reaction
    作者:Talapaneni,Siddulu Naidu; Park,Dae-Hwan; Choy,Jin-Ho; Ramadass,Kavitha; Elzatahry,Ahmed; Et Al
    参考文献:Chemistryselect 日期:2016 卷标:1(19) 页码:6062-6068]

    98-86-2 + 71-36-3 = 942-92-7
    反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Palladium,Aluminum Hydroxide Solvents: Toluene; 12 H,80 °C
    标题:Recyclable Palladium Catalyst For Highly Selective α-Alkylation Of Ketones With Alcohols
    作者:Kwon,Min Serk; Kim,Namdu; Seo,Seong Hyeok; Park,In Soo; Cheedrala,Ravi Kumar; Et Al
    参考文献:Angewandte Chemie 日期:2005 卷标:44(42) 页码:6913-6915]

    98-80-6 + 19337-31-6 = 942-92-7
    反应条件:1.1 Catalysts: Triphenylphosphine,2920169-35-1 (Reaction Product With Iron Oxide) Solvents: 1,4-Dioxane; 5 H,50 °C
    标题:Preparation And Characterization Of A Magnetic Catalyst For Coupling Reactions
    作者:Pan,Peiling; Mohammadnia,Majid
    参考文献:Journal Of Coordination Chemistry 日期:2023 卷标:76(3-4) 页码:467-478]

    190523-59-2 = 942-92-7
    反应条件:1.1 Reagents: 2-Methyl-2-Butene,Monosodium Phosphate,Sodium Chlorite Solvents: Methanol,Water; Rt; Rt -> 0 °C; 3 H,Rt
    标题:Oxidative Deprotection Of 1,3-Dithiane Group Using Naclo2 And Nah2Po4 In Aqueous Methanol
    作者:Ichige,Takahiro; Miyake,Annu; Kanoh,Naoki; Nakata,Masaya
    参考文献:Synlett 日期:2004 卷标:(10) 页码:1686-1690]

    70-11-1 = 942-92-7
    反应条件:1.1 Reagents: Potassium Tert-Butoxide
    标题:Formation Of Carbon-Carbon And Carbon-Heteroatom Bonds Via Organoboranes And Organoborates
    作者:Negishi,Ei-Ichi; Idacavage,Michael J.
    参考文献:Organic Reactions (Hoboken 日期:1985 卷标:33]

    4471-05-0 = 942-92-7
    反应条件:1.1 Reagents: Sulfuric Acid Magnesium Salt (1:1),Oxygen Catalysts: Vanadyl Sulfate,4,4′-Bis(1,1-Dimethylethyl)-2,2′-Bipyridine Solvents: Water; 120 H,90 °C
    标题:Vanadium-Catalyzed Green Oxidation Of Benzylic Alcohols In Water Under Air Atmosphere
    作者:Marui,Kuniaki; Higashiura,Yuuki; Kodama,Shintaro; Hashidate,Suguru; Nomoto,Akihiro; Et Al
    参考文献:Tetrahedron 日期:2014 卷标:70(14) 页码:2431-2438]

    82777-11-5 = 942-92-7
    反应条件:1.1 Reagents: Oxygen,Dibutylchlorogermane Catalysts: Triethylborane Solvents: Tetrahydrofuran,Hexane; 1 H,0 °C -> Rt
    标题:Synthetic Radical Reactions Using Dibutylchlorogermane And Dibutylethoxygermane As Radical Mediators
    作者:Miura,Katsukiyo; Ootsuka,Kazunori; Hosomi,Akira
    参考文献:Synlett 日期:2005 卷标:(20) 页码:3151-3153]

    98-86-2 + 71-36-3 = 942-92-7
    反应条件:1.1 Reagents: Sodium Hydroxide Catalysts: Iridium,Di-μ-Chlorodichlorobis[(1,2,3,4,5-η)-1,2,3,4,5-Pentamethyl-2,4-Cyclopen... Solvents: Toluene; 17 H,110 °C
    标题:Direct β-Alkylation Of Secondary Alcohols With Primary Alcohols Catalyzed By A Cpir Complex
    作者:Fujita,Kenichi; Asai,Chiho; Yamaguchi,Tetsuhiro; Hanasaka,Fumihiro; Yamaguchi,Ryohei
    参考文献:Organic Letters 日期:2005 卷标:7(18) 页码:4017-4019
己酸置于4-二甲氨基吡啶,1,10-邻菲啰啉二溴化镍,二氢吡啶,N,N'-二环己基碳二亚胺,Lithium Bromide体系中,用 四氢呋喃,N,N-二甲基乙酰胺 作为反应溶剂,化学反应 48.0H,反应生成 苯己酮
参考文献:用于酮合成的镍介导的羧酸衍生物光还原交叉偶联**
标题:用于酮合成的镍介导的羧酸衍生物光还原交叉偶联**
摘要:介导合成:提出了一种使用可见光和两种羧酸衍生底物镍催化合成酮的策略.不需要昂贵的铱催化剂,环保的 Hantzsch 酯既充当光敏剂又充当光还原剂.介绍了广泛的合成酮以及不同反应物作用的光谱和计算研究.
DOI:10.1002/chem.202103486

海关参考信息

专利信息


专利号:US-6066705-A
优先权日:1995-08-31
标 题 :Vapor phase synthesis of cis-1, 4-Polyisoprene
发明人:CALDERON NISSIM; CASTNER KENNETH FLOYD; COLVIN HOWARD ALLEN; MUSE JR JOEL
权利人:GOODYEAR TIRE & RUBBER
摘要:By utilizing the vapor phase polymerization techniques of the present invention, numerous distinct and highly beneficial advantages are realized. For instance, cis-1,4-polyisoprene rubber and high cis-1,4-polybutadiene rubber having a consistent and controllable molecular weight can be easily and practically prepared without utilizing a solvent. The subject invention more specifically discloses a method for vapor phase polymerizing isoprene into cis-1,4-polyisoprene in a process comprising the steps of: (1) charging into a reaction zone said isoprene and a preformed catalyst system which is made by reacting an organoaluminum compound with titanium tetrachloride, preferably in the presence of at least one ether; wherein the isoprene is maintained in the vapor phase in said reaction zone by a suitable combination of temperature and pressure; (2) allowing said isoprene to polymerize into cis-1,4-polyisoprene at a temperature within the range of about 35 DEG C. to about 70 DEG C.; and (3) withdrawing said cis-1,4-polyisoprene from said reaction zone. It has been determined that gel formation can be reduced by conducting the polymerization of isoprene monomer in the presence of a diarylamine, such as para-styrenated diphenylamine.

专利号:US-5859156-A
优先权日:1995-08-31
标 题 :Vapor phase synthesis of rubbery polymers
发明人:CALDERON NISSIM; MUSE JR JOEL; COLVIN HOWARD ALLEN; CASTNER KENNETH FLOYD
权利人:GOODYEAR TIRE & RUBBER
摘要:By utilizing the vapor phase polymerization techniques of the present invention, numerous distinct and highly beneficial advantages are realized. For instance, cis-1,4-polyisoprene rubber and high cis-1,4-polybutadiene rubber having a consistent and controllable molecular weight can be easily and practically prepared without utilizing a solvent. The subject invention more specifically discloses a method for vapor phase polymerizing isoprene into cis-1,4-polyisoprene in a process comprising the steps of: (1) charging into a reaction zone said isoprene and a preformed catalyst system which is made by reacting an organoaluminum compound with titanium tetrachloride, preferably in the presence of at least one ether; wherein the isoprene is maintained in the vapor phase in said reaction zone by a suitable combination of temperature and pressure; (2) allowing said isoprene to polymerize into cis-1,4-polyisoprene in said reaction zone at a temperature within the range of about 0 DEG C. to about 100 DEG C. in the presence of a diarylamine, wherein said reaction zone is a horizontal, stirred reactor of substantially circular cross section containing a centrally-located drive shaft extending longitudinally through said reactor to which are attached a plurality of adjacently located paddles, which paddles cause essentially no forward or backward movement of the cis-1,4-polyisoprene contained in said reactor; and (3) withdrawing said cis-1,4-polyisoprene from said reaction zone.

专利号:US-3883591-A
优先权日:1969-02-26
标 题:Intermediates for the preparation of 1,3-dihydro-2H-1,4-benzodiazepin-2-ones
发明人:MCCAULLY RONALD J
权利人:AMERICAN HOME PROD
摘要:Two routes for the preparation of 2-(2-acylamido-2-amino)acetamidophenyl aryl ketones, used as intermediates in the synthesis of psycholeptic 1,3-dihydro-2H-1,4-benzodiazepin-2-ones are described. The first of these routes involves the formation of a 2-(2,2-diacyloxy)acetamidophenyl aryl ketone from glyoxylic acid and an aryl phenyl ketone via either a 2,2-diacyloxy acetyl halide or a 2,2-diacyloxy acetyl anhydride, coversion thereof to the corresponding 2-(2-acylamido-2-hydroxy) acetamidophenyl aryl ketone directly or via the 2-(2,2-dihydroxy)acetamidophenyl aryl ketone, formation of the corresponding 2-(2-acylamido-2halo)acetamidophenyl aryl ketone, and conversion to the 2-(2acylamido-2-amino)acetamidophenyl aryl ketone. The second route forms the 2-(2,2-dihydroxy)acetamidophenyl aryl ketone by reacting a 2,3-dicarboxylicacyl tartaric anhydride with a 2aminophenyl aryl ketone to obtain a 2-(3-carboxy-2,3acyloxy)propionamidophenyl aryl ketone, selectively hydrolyzing the so-obtained ketone and selectively oxidizing the product with a vic glycol cleaving agent.

专利号:US-7081504-B2
优先权日:2004-08-30
标 题:Synthesis of 1,4-polybutadiene
发明人:RACHITA MICHAEL JOSEPH; JOHNSON SCOTT EDWARDS
权利人:GOODYEAR TIRE & RUBBER
摘要:This invention is based upon the unexpected discovery that alkylated diphenylamines can be used in conjunction with nickel based catalyst systems which contain (a) an organonickel compound, (b) an organoaluminum compound, and (c) a fluorine containing compound to produce cis-1,4-polybutadiene having reduced molecular weight and an increased level of branching. This results in the cis-1,4-polybutadiene exhibiting good processability without sacrificing cold flow characteristics. Additionally, the alkylated diphenylamine which remains in the rubber acts in a manner which provides it with antioxidant protection. In other words, the use of alkylated diphenylamines accomplishes the three major objectives that are realized by employing para-styrenated diphenylamines (reduced molecular weight, regulated polymer macrostructure through branching and antidegradant protection). However, the utilization of alkylated diphenylamines, unlike para-styrenated diphenylamines, offers the additional advantage of being soluble in aliphatic solvents. By virtue of this increased level of solubility in aliphatic solvents, such as hexane, alkylated diphenylamines can be employed at greatly reduced levels of aromatic solvents. Likewise, when mixed catalyst streams containing alkylated diphenyl amines are combined precipitation is minimized compared to para-styrenated diphenylamine significantly improving issues related to fouling. The subject invention more specifically discloses a process for producing cis-1,4-polybutadiene having a reduced molecular weight and improved processability which comprises polymerizing 1,3-butadiene in the presence of (a) an organonickel compound, (b) an organoaluminum compound, (c) a fluorine containing compound, and (d) an alkylated diphenylamine; wherein the alkylated diphenylamine has alkyl groups that contain from 2 to 18 carbon atoms, and wherein the organoaluminum compound and the fluorine containing compound are brought together in the presence of the alkylated diphenylamine.

专利号:US-3899527-A
优先权日:1969-02-26
标题:Intermediates for the preparation of 1,3-dihydro-2H-1,4-benzodiazepin-2-ones
发明人:MCCAULLY RONALD J
权利人:AMERICAN HOME PROD
摘要:Two routes for the preparation of 2-(2-acylamido-2-amino)acetamidophenyl aryl ketones, used as intermediates in the synthesis of psycholeptic 1,3-dihydro-2H-1,4-benzodiazepin-2-ones are described. The first of these routes involves the formation of a 2-(2,2-diacyloxy)acetamidophenyl aryl ketone from glyoxylic acid and an aryl phenyl ketone via either a 2,2-diacyloxy acetyl halide or a 2,2-diacyloxy acetyl anhydride, conversion thereof to the corresponding 2-(2-acylamido-2-hydroxy) acetamidophenyl aryl ketone directly or via the 2-(2,2-dihydroxy)acetamidophenyl aryl ketone, formation of the corresponding 2-(2-acylamido-2halo)acetamidophenyl aryl ketone, and conversion to the 2-(2acylamido-2-amino)acetamidophenyl aryl ketone. The second route forms the 2-(2,2-dihydroxy)acetamidophenyl aryl ketone by reacting a 2,3-dicarboxylicacyl tartaric anhydride with a 2aminophenyl aryl ketone to obtain a 2-(3-carboxy-2,3acyloxy)propionamidophenyl aryl ketone, selectively hydrolyzing the so-obtained ketone and selectively oxidizing the product with a vic glycol cleaving agent.

专利号:US-7517828-B2
优先权日:2003-04-25
标 题 :Chiral broensted acid catalyst for asymmetric synthesis and method of asymmetric synthesis with the catalyst
发明人:AKIYAMA TAKAHIKO
权利人:TOAGOSEI CO LTD
摘要:A compound usable as an asymmetric synthesis catalyst which can be easily synthesized without using any metal such as a lanthanoid group element; a method of asymmetric synthesis with the compound; and a chiral compound obtained by the asymmetric synthesis method. A Broensted acid is used as a catalyst in asymmetric synthesis, the chiral Broensted acid being represented by formula (1) below or formula (3) below. The asymmetric synthesis method employs the catalyst. Asymmetric synthesis with the catalyst gives a chiral compound.
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✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: Martin Gilar, Et Al. Repetitive Injection Method: A Tool For Investigation Of Injection Zone Formation And Its Compression In Microfluidic Liquid Chromatography. J Chromatogr A. 2015 Feb 13:1381:110-7.
[参考文献]: Martin Gilar, Et Al. Wide Injection Zone Compression In Gradient Reversed-Phase Liquid Chromatography. J Chromatogr A. 2015 Apr 17:1390:86-94.

合成参考文献


摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 163.
摘要:Sellars, J. D., Science of Synthesis Knowledge Updates, (2014) 1, 440.
摘要:De Wildeman, S.; Sereinig, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 160.
摘要:Guram, A. S.; Milne, J. E.; Tedrow, J. S.; Walker, S. D., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 115.
摘要:Liu, S.; Xiao, J., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 251.
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