CAS: 1823-91-2; 2-Phenylpropanenitrile

该化合物是一个有机化合物,其特点是附于一个苯和丙基组的硝化物功能组,其典型的颜色无色,可视温度和纯度而定,为黄色液体或固态;该化合物的分子式为C10H11N,表明含有10个碳原子,11个氢原子和1个氮原子. 2-苯丙基丙酰三联因其芳香特性而闻名,因为有苯基组的存在,可影响其再活动及与其他物质的互动;该化合物经常用于有机合成,可作为生产药品和农用化学品的中间体;该化合物一般在标准条件下稳定,但因与硝酸盐相关的潜在毒性和刺激性而应谨慎处理;建议采取适当的安全措施,包括使用个人防护设备,在与该物质合作时,包括使用个人防护设备.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

CAS号34713-70-7 2-苯基丙醛 | CAS号1617-17-0 2-氯丙腈 | CAS号368-47-8 苯基三氟硅烷 | CAS号292638-84-7 phenylene-ethylene | CAS号75-86-5 丙酮氰醇 | CAS号140-29-4 苯乙腈 | CAS号74-88-4 碘甲烷 | CAS号492-37-5 2-苯基丙酸 | CAS号1125-70-8 2-苯基丙酰胺 | CAS号672-65-1 1-氯-1-苯乙烷 | CAS号2049-80-1 烯丙基丙二酸二乙酯 | CAS号3195-24-2 二烯丙基丙二酸二乙酯 | CAS号5591-70-8 3-氨基-4-苯基-1H-吡唑 | CAS号50712-63-5 2-(4-硝基苯基)丙腈 | CAS号34298-25-4 (R)-beta-甲基苯乙胺盐酸盐 | CAS号5961-33-1 3-甲基-3-苯基氮杂啶 | CAS号1425-59-8 2-Methyl-2-phen... | CAS号492-37-5 2-苯基丙酸 | CAS号7782-24-3 (|S|)-(+)-2-苯丙酸 | CAS号7782-26-5 R-2-苯基丙酸

合成工艺路线路线简述

    2-Phenylpropanamide置于光气体系中,用 四氢呋喃,甲苯 用作溶剂,化学反应 4.0H,以82%的收率获得α-甲基苯腈
    参考文献:从相应的酰胺或腈合成 1-芳基-2-氨基链烷醇衍生物的一锅法
    标题:从相应的酰胺或腈合成 1-芳基-2-氨基链烷醇衍生物的一锅法
    摘要:我们已经确定了一种用于合成 β-氨基醇的新型一锅法,该方法基于苄基 α-碳原子上的 C-H 键羟基化,随后腈或酰胺官能团还原.这种级联过程使用分子氧作为氧化剂和双(2-甲氧基乙氧基)氢化铝钠作为还原剂.对 30 个条目检查了底物范围,尽管相应产品仅以中等产率提供,但上述简单方案可作为其他难以制备的空间拥挤 1,2-氨基醇的直接且有力的入口路线.给出了观察结果的合理机械原理,并将反应应用于潜在生物活性靶标的合成.
    Doi:10.1039/d0Ra04359A

    海关参考信息

    专利信息


    专利号:WO-2014202765-A1
    优先权日:2013-06-21
    标题 :Preparation of chiral 1-methyl-2,3,4,5-1h-benzodiazepines via asymmetric reduction of alpha-substituted styrenes
    发明人:STAVBER GAJ; GAZIC SMILOVIC IVANA; CLUZEAU JEROME; RICHTER FRANK
    权利人:LEK PHARMACEUTICALS
    摘要:The present invention provides an asymmetric and economic synthesis of 8-chloro-1-methyl-2,3,4,5-tetrahydro-1 H-benzo[d]azepine via novel intermediates applying an asymmetric enzymatic, biomimetic or catalytic reduction. The present invention also provides a novel green asymmetric catalytic reduction adapted for an aqueous medium to be applied in the synthesis of 8-chloro-1-methyl-2,3,4,5-tetrahydro-1 H-benzo[d]azepine or novel intermediates.

    专利号:US-6048991-A
    优先权日:1990-11-16
    标题:Preparation of epoxides
    发明人:HAERMELING DIETER
    权利人:BASF AG
    摘要:Alpha-hydroxy-epoxides of alpha-alkoxy-epoxides of the formula IV ##STR1## in which the substituents have the following meanings: R 7 , R 8 , R 9 , R 10 , R 11 are independently hydrogen, C 1 -C 20 -alkyl, C 3 -C 12 -cycloalkyl, C 4 -C 20 -cycloalkylalkyl, C 1 -C 20 -hydroxy-alkyl, a heterocyclic ring, or an aryl or C 7 -C 20 -arylalkyl group optionally substituted by C 1 -C 8 -alkyl, C 1 -C 8 -alkoxy, halogen, C 1 -C 4 -haloalkyl, C 1 -C 4 -halo-alkoxy, phenyl, phenoxy, halophenyl, halophenoxy, carboxy, C 2 -C 8 -alkoxycarbonyl, or cyano, or R 7 and R 8 or R 7 and R 9 or R 7 and R 10 or R 9 and R 10 or R 10 and R 11 together form a (CH 2 ) n group in which n is an integer from 1 to 10 and which may be optionally substituted by C 1 -C 8 -alkyl, C 1 -C 8 -alkoxy, and/or halogen, and n R 12 is hydrogen, C 1 -C 8 -alkyl, or benzyl, n provided that R 10 is not hydrogen, methyl, ethyl, propyl, or cyclohexyl when R 7 , R 8 , R 9 , or R 11 is hydrogen, that R 7 is not methyl when R 8 is methyl or phenyl and R 9 , R 10 , or R 11 is hydrogen, that R 7 is not methyl when R 8 , R 9 , R 10 , or R 11 is hydrogen and R 12 is ethyl, that R 7 is not phenyl or hexyl when R 8 , R 9 , R 10 , or R 11 is hydrogen, that R 9 is not methyl when R 7 , R 8 , R 10 , or R 11 is hydrogen, that R 10 and R 11 are not methyl when R 7 , R 8 , or R 9 is hydrogen, and that R 7 and R 10 do not together form an unsubstituted cycloalkyl when R 8 , R 9 , or R 11 is hydrogen. The epoxides of the above formula serve as intermediates for the synthesis of, inter alia, perfumes, plant protectants and polymers.

    专利号:US-7605290-B2
    优先权日:2006-07-26
    标题 :Processes for the synthesis of O-desmethylvenlafaxine
    发明人:NIDDAM-HILDESHEIM VALERIE; SHENKAR NATALIA; SHACHAN-TOV SHARONA
    权利人:TEVA PHARMA
    摘要:The present invention describes processes for the preparation of O-desmethylvenlafaxine and tridesmethylvenlafaxine, which may be used as an intermediate in preparing O-desmethylvenlafaxine.

    专利号:US-2009069601-A1
    优先权日:2006-07-26
    标题:Processes for the synthesis of O-desmethylvenlafaxine
    发明人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION
    权利人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION
    摘要:The present invention describes processes for the preparation of O-desmethylvenlafaxine and tridesmethylvenlafaxine, which may be used as an intermediate in preparing O-desmethylvenlafaxine.

    专利号:US-2008221356-A1
    优先权日:2006-07-26
    标题:Processes for the synthesis of O-desmethylvenlafaxine
    发明人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION
    权利人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION
    摘要:The present invention describes processes for the preparation of O-desmethylvenlafaxine and tridesmethylvenlafaxine, which may be used as an intermediate in preparing O-desmethylvenlafaxine.

    专利号:US-2009137846-A1
    优先权日:2006-07-26
    标题 :Processes for the synthesis of O-Desmethylvenlafaxine
    发明人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION; FRENKEL GUSTAVO
    权利人:NIDDAM-HILDESHEIM VALERIE; NIDAM TAMAR; DOLITZKY BEN-ZION; FRENKEL GUSTAVO
    摘要:The present invention describes processes for the preparation of O-desmethylvenlafaxine and tridesmethylvenlafaxine, which may be used as an intermediate in preparing O-desmethylvenlafaxine.
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    主要参考文献

    参考标题:Fe(Clo4)3.H2O-Catalyzed Ritter Reaction: A Convenient Synthesis Of Amides From Esters And Nitriles
    作者:Min Ji,Chengliang Feng,Bin Yan,Guibo Yin,Junqing Chen |发布日期:2018.10
    摘要:An Efficient And Inexpensive Synthesis Of N-Substituted Amides From The Ritter Reaction Of Nitriles With Esters Catalyzed By Fe(Clo4)3.H2O Is Described. Fe(Clo4)3.H2O Is An Economically Efficient Catalyst For The Ritter Reaction Under Solvent-Free Conditions. Reactions Of A Range Of Esters (Benzyl, Sec-Alkyl, And Tert-Butyl Esters) With Nitriles (Primary, Secondary, Tertiary, And Aryl Nitriles) Were

    合成参考文献


    摘要:Chciuk, T. V.; Flowers, R. A.; Flowers, R. A., Science of Synthesis Knowledge Updates, (2016) 2, 232.
    摘要:Spitzner, D., Science of Synthesis Knowledge Updates, (2016) 1, 36.
    摘要:van Leeuwen, P. W. N. M., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 451.
    摘要:Tauchert, M. E., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 1, 312.
    摘要:Tauchert, M. E., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 1, 330.
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