CAS: 1586-00-1; (2-Benzylphenyl)Methanol

该化合物是一种双功能芳香醇,其特征是存在一种苯基和与苯环相连的氢氧基混合物,这种结构具有主要酒精的典型反应性,使其成为有机合成的多用途中间体,特别是用于生产药品,香料和特殊化学品.其双重功能允许选择性转化,如酯化或发酵,而芳香骨干则增强稳定性.复合体在极地有机溶剂中表现出中等溶性,便于在同质反应系统中使用.由于对氧化的潜在敏感性,建议进行适当处理.建议在惰性条件下储存保持纯度.

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合成工艺路线路线简述

    📜2-甲基二苯甲酮置于chromium(Vi) Oxide,盐酸,Lithium Aluminium Tetrahydride,硫酸,溶剂黄146,汞,锌体系中,用 乙醚 用作溶剂,化学反应生成2-苄基苯甲醇
    参考文献:Chemistry And Stereochemistry Of Benzyl-Benzyl Interactions In Mh+ Ions Of Dibenzyl Esters Upon Chemical Ionization And Collision-Induced Dissociation Conditions
    标题:Chemistry And Stereochemistry Of Benzyl-Benzyl Interactions In Mh+ Ions Of Dibenzyl Esters Upon Chemical Ionization And Collision-Induced Dissociation Conditions
    摘要:Isobutane Chemical Ionization Mass Spectra Of Dibenzyl Esters Of A Wide Variety Of Aliphatic,Olefinic,Alicyclic And Aromatic Dicarboxylic Acids Exhibit Abundant M/z 181 C14H13+ Ions,Indicating A Highly General Rearrangement Process Involving The Formation Of A New Bond Between The Two Benzyl Groups. An Extensive Collision-Induced Dissociation And Deuterium Labeling Study Suggested That These Ions Are An Almost Equimolar Mixture Of Isomeric Alpha-O-Tolylbenzyl,Alpha-P-Tolylbenzyl And P-Benzylbenzyl Cation Structures,And This Composition Is Identical For All The Diesters Examined This Structural Assignment Of The C14H13+ Ions Suggests A Mechanistic Pathway For Their Generation,Based On The Formation Of The New Bond Between Tbe Benzyl Methylene Group Of The Protonated Benzoxycarbonyl And The Phenyl Ring Of The Otter Ester Moiety Via Pi-(And/or Ion-Neutral) And A-Complexes. Stereoisomeric Diesters Show An Unusual Steric Effect: Trans-Isomers Give Rise To Much More Abundant C14H13+ Ions Than The Cis Counterparts,This Behavior Is Explained By Stabilized Proton-Bridged Structures Of The Mh+ Ions Of The Cis-Isomers. (C) 1997 By John Wiley & Sons,Ltd.
    Doi:10.1002/(Sici)1096-9888(199705)32:5<515::Aid-Jms504>3.0.Co;2-B

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/bf00767069
    摘要:Sreekumar R, Pillai CN. Reactions of benzyl alcohol and dibenzyl ether over zeolites. Catalysis Letters. 1993 Dec;19(4):281–91. doi: 10.1007/bf00767069.
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