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2,6-二叔丁基-4-甲基苯酚 2,6-Di-Tert-Butyl-4-Methyl-Phenol 128-37-0
2,6-二叔丁基苯酚 2,6-Di-T-Butylphenol 128-39-2合成工艺路线路线简述
- 128-39-2 = 88-27-7
反应条件:1.1 Solvents: Ethanol,Water
标题:Heterocyclic Spirocyclohexadienones From Substituted Phenols
作者:Moehrle,H.; Et Al
参考文献:Zeitschrift Fuer Naturforschung 日期:1995 卷标:50(12) 页码:1859-68]
955-01-1 = 88-27-7
反应条件:1.1 1 H,Reflux
标题:Preparation Of Chloro- And Aminomethyl Derivatives Of Sterically Hindered Phenols
作者:Guseinov,I. Sh.; Et Al
参考文献:Azerbaidzhanskii Khimicheskii Zhurnal 日期:2007 卷标:(4) 页码:114-117]
128-39-2 = 88-27-7
反应条件:1.1 Reagents: Acetic Acid Solvents: Water; 4 H,Reflux; Cooled
标题:Synthesis And Hepatoprotector Activity Of Water-Soluble Derivatives Of Aminoalkylphenols
作者:Dyubchenko,O. I.; Et Al
参考文献:Pharmaceutical Chemistry Journal 日期:2006 卷标:40(5) 页码:243-247]
2091-51-2 = 88-27-7
反应条件:1.1 Solvents: Tetrahydrofuran; 2 H,273 K
标题:2,6-Di-Tert-Butyl-4-(Dimethylaminomethyl)Phenol
作者:Zeng,Tao; Et Al
参考文献:Acta Crystallographica 日期:2008 卷标:64(1)]
955-01-1 = 88-27-7 [标题:Reaction Conditions
标题:Synthesis And Antioxidative Properties Of Some 2,6-Di-Tert-Butyl-4-Aminomethylphenols
作者:Guliev,F. A.; Et Al
参考文献:Azerbaidzhanskii Khimicheskii Zhurnal 日期:1998 卷标:(1) 页码:93-96]
128-37-0 = 88-27-7
反应条件:1.1 Reagents: Tert-Butyl Hydroperoxide,Quinoline N-Oxide,Oxygen Catalysts: Cuprous Iodide Solvents: Dichloromethane,Decane; 40 °C
标题:Cu-Catalyzed Carbamoylation Versus Amination Of Quinoline N-Oxide With Formamides
作者:Zhang,Yan; Et Al
参考文献:Organic & Biomolecular Chemistry 日期:2019 卷标:17(2) 页码:309-314]
128-39-2 = 88-27-7
反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Water; Rt1.2 Solvents: Carbon Tetrachloride; 1 - 1.5 H,Rt; Rt -> 45 °C; 3 - 4 H,40 - 45 °C2.1 1 H,Reflux
标题:Preparation Of Chloro- And Aminomethyl Derivatives Of Sterically Hindered Phenols
作者:Guseinov,I. Sh.; Et Al
参考文献:Azerbaidzhanskii Khimicheskii Zhurnal 日期:2007 卷标:(4) 页码:114-117]
128-39-2 = 88-27-7
反应条件:1.1 Reagents: Hydrochloric Acid2.1 -
标题:Synthesis And Antioxidative Properties Of Some 2,6-Di-Tert-Butyl-4-Aminomethylphenols
作者:Guliev,F. A.; Et Al
参考文献:Azerbaidzhanskii Khimicheskii Zhurnal 日期:1998 卷标:(1) 页码:93-96
2,6-二叔丁基-4-甲基苯酚,N,N-二甲基甲酰胺置于叔丁基过氧化氢,喹啉-N-氧化物,Copper(I) Bromide体系中,用 癸烷,二甲基亚砜 作为反应溶剂,化学反应生成 2,6-二叔丁基对(二甲氨甲基)苯酚
参考文献:铜-催化的氨基甲酰化与喹啉的胺化ñ与甲酰胺氧化物
标题:铜-催化的氨基甲酰化与喹啉的胺化ñ与甲酰胺氧化物
摘要:通过铜催化的c-C和c-N键的形成,通过交叉脱氢偶联反应,已开发出一种高效,直接的氨基甲酰基化和喹啉n-氧化物与甲酰胺的胺化反应,以反应生成2-氨基甲酰基和2-氨基喹啉.在温和条件下,该反应可在广泛的具有非常好官能团耐受性的底物上顺利进行.机理研究表明,根据甲酰胺n原子上不同的取代基,在tbhp存在下,该反应是由甲酰胺基或脱羰基氨酰基自由基的形成引发的.
DOI:10.1039/c8Ob02844C
海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2907121100-间甲酚
2908199090-其他酚的卤化衍生物 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-6329543-B1
优先权日:1999-05-06
标题:Process for synthesis of isobornyl (Meth) acrylate
发明人:KNEBEL JOACHIM; SAAL DORIS
权利人:ROEHM GMBH
摘要:The present invention relates to processes for synthesis of isobornyl (meth)acrylate by reacting camphene with (meth)acrylic acid in the presence of sulfuric acid and at least one compound having inhibiting action. Aqueous sulfuric acid with an acid concentration in the range of 65 to 85 wt % is used. Isobornyl (meth)acrylate can advantageously be distilled from a mixture containing sulfuric acid in the presence of 2,6-di-tert-butyl-alpha-(dialkylamino)-p-cresol.
专利号:US-2009318592-A1
优先权日:2005-10-11
标 题 :Process for the Synthesis of Amine Ethers
发明人:FREY MARKUS; BROENNIMANN VALERIE
权利人:CIBA GEIGY CORP
摘要:The present invention relates to novel processes for the preparation of a sterically hindered amine ether by reacting a corresponding sterically hindered amine oxide with a ketone or an aldehyde with at least one reactive H in the presence of a peroxydisulphate. Products obtained by this process may be hydrogenated. The compounds made by these processes are particularly effective in the stabilization of polymer compositions against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.
专利号:US-2007191516-A1
优先权日:2004-03-15
标题 :Process for the synthesis of amine ethers
发明人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
权利人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
摘要:A process for the preparation of a sterically hindered amine ether which comprises reacting a corresponding sterically hindered aminoxide with a C 5 -C 18 alk-1-ene in the presence of an organic hydroperoxide and optionally hydrogenating the resulting product as well as the product mixtures obtained therewith and their use as stabilizers and flame retardants.
专利号:US-2023047214-A1
优先权日:2020-02-03
标题:Methods for microwave synthesis of degradable polymers for drug delivery
发明人:MURATOGLU ORHUN K; ORAL EBRU; GRINDY SCOTT
权利人:MASSACHUSETTS GEN HOSPITAL
摘要:Provided herein are methods of making degradable, additive-blended polymeric materials using microwave radiation and catalysts. The methods can include incorporation of therapeutic materials into the polymeric materials. There also are provided polymeric materials made by the methods and medical devices comprising the polymeric materials made by the methods.
专利号:US-7402675-B2
优先权日:2000-05-26
标题 :Process for the synthesis of amine ethers from secondary amino oxides
发明人:HAFNER ANDREAS; KIRNER HANS JUERG; SCHWARZENBACH FRANZ; VAN DER SCHAAF PAUL ADRIAAN; NESVADBA PETER
权利人:CIBA SC HOLDING AG
摘要:An amine ether of formula A n nwherein a is 1 or 2; and when a is 1, E is E′; when a is 2, E is L;n E′ is C 1 -C 36 alkyl; C 3 -C 18 alkenyl; C 2 -C 18 alkinyl; C 5 -C 18 cycloalkyl; C 5 -C 18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or tricyclic hydrocarbon of 7 to 12 carbon atoms; C 2 -C 7 alkyl or C 3 -C 7 alkenyl substituted by halogen; C 7 -C 15 aralkyl or C 7 -C 15 aralkyl substituted by C 1 -C 4 alkyl or phenyl; or E′ is a radical of formula (VII) as explained in claim 1; T′ is tertiary C 4 -C 18 alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR 21 or C(O)—R 22 ; or T′ is C 5 -C 12 cycloalkyl; C 5 -C 12 cycloalkyl which is interrupted by at least one O or —NR 18 —; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or —NR 18 —; or T′ is —C(G 1 )(G 2 )-T″; or C 1 -C 18 alkyl or C 5 -C 12 cycloalkyl substituted by n n n n n n n n n n n n T″ is hydrogen, halogen, NO 2 , cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; n or T″ and T′ together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G 1 and G 2 , an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, n are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E 1 -H or H-L-H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. n n n n n The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.
专利号:US-6417363-B1
优先权日:1997-12-04
标题 :Heterocyclyl ligand containing ruthenium and osmium catalysts
发明人:VAN DER SCHAAF PAUL ADRIAAN; MUEHLEBACH ANDREAS; HAFNER ANDREAS; KOLLY ROMAN
权利人:CIBA SC HOLDING AG
摘要:Penta- and hexa-coordinated, bridged ruthenium and osmium catalysts of the formulawherein Me is ruthenium or osmium; L1 and L2 are neutral ligands having electron donor properties;X is an anionic ligand; Y is oxygen or sulphur; A is a direct bond, C1-C4alkylene or C2-C4alkylidene;Z is a direct bond, oxygen, sulphur or the groupswherein R1 and R2 are hydrogen or hydrocarbon radicals; their preparation and their us in the synthesis of polymers, in the ring-closure metathesis of diolefins, in the cross metathesis of olefins and in the isomerisation of olefins are disclosed.