CAS: 57337-85-6; P-(Trimethylsilyl)Phenylmethanethiol

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    (4-(bromomethyl)phenyl)trimethylsilane thiourea para-bromotoluene p-(trimethylsilyl)toluene5-(4-trimethylsilanyl-benzylsulfanyl)-hexan-3-one 3-methyl-3-(4-trimethylsilanyl-benzylsulfanyl)-butyric acid ethyl ester 2-methyl-3-(4-trimethylsilanyl-benzylsulfanyl)-propionic acid ethyl ester 3-(4-trimethylsilanyl-benzylsulfanyl)-butyric acid ethyl ester

    合成工艺路线路线简述

      📜1-溴甲基-4-三甲基甲硅烷基-苯置于硫脲,Sodium Hydroxide体系中,用71%的收率获得产物4-(三甲基硅烷基)苯甲硫醇
      参考文献:Synthetic Equivalents Of Benzenethiol And Benzyl Mercaptan Having Faint Smell: Odor Reducing Effect Of Trialkylsilyl Group
      标题:Synthetic Equivalents Of Benzenethiol And Benzyl Mercaptan Having Faint Smell: Odor Reducing Effect Of Trialkylsilyl Group
      摘要:Syntheses And Odor Tests Of The Trialkylsilylated Benzyl Mercaptans And Benzenethiols Have Revealed That The Trimethylsilyl Substituent On The Benzene Ring Has A Remarkable Effect In Reducing The Foul Smell Of The Parent Benzyl Mercaptan And Benzenethiol. Protodesilylation Allowed These Silylated Thiols To Function As Odorless Synthetic Equivalents Of Benzyl Mercaptan And Benzenethiol. This Discovery Will Greatly Improve The Physical Environment Of The Researcher Working With These Malodorous Compounds. (C) 2002 Elsevier Science Ltd. All Rights Reserved.
      DOI:10.1016/s0040-4039(02)02052-X

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      ✅ COA系统入驻 | 共享模式

      合成参考文献

      合成方法参考DOI号:10.1007/s00706-003-0122-1
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