CAS: 453-11-2; 1-Chloro-3-Fluoropropan-2-Ol

该化合物是有机化合物,其特点是三碳醇结构中含有氯和氟原子,这种化合物一般看起来无色,不光彩,不光彩黄色液体,由于氢氧(-OH)组具有极性,它具有极性,有助于其在水和其他极溶剂中的溶解性.卤素,特别是氯和氟,会影响它的再活动,使它成为各种化学反应,包括核生殖替代的潜在候选物.这种化合物经常用于有机合成,并可作为生产药品或农用化学品的一个中间体.在处理这种化合物时,安全考虑十分重要,因为它可能会通过吸入或皮肤接触造成健康风险.应当遵循适当的储存和处理规程,以减少与使用该化合物有关的任何潜在危害.

结构式图片

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19141-39-0 37493-16-6

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上下游产品

epichlorohydrin 1,3-Dichloro-2-propanol 1,2-Dichloropropane 1-Chloro-3-fluoro-prop-2-one Guajacyl-(2-hydroxy-3-fluor-propyl)-aether 1-Fluoro-3-phenoxypropan-2-ol Fluoromisonidazole

合成工艺路线路线简述

    📜环氧氟丙烷置于sodium Chloride体系中,用 Aq. Acetate Buffer 作为反应溶剂,化学反应 1.0H,以63%的收率获得产物1-氯-3-氟-2-丙醇
    参考文献:Halohydrin Dehalogenase-Catalysed Transformations Of Epifluorohydrin
    标题:Halohydrin Dehalogenase-Catalysed Transformations Of Epifluorohydrin
    摘要:Biocatalytic Ring-Opening Of Epifluorohydrin Has Been Performed By Using Halohydrin Dehalogenase. The Enzyme From Mycobacterium Sp. Gp1 (Hheb2) Catalysed Reaction With High Regioselectivity And Low Enantioselectivity In The Presence Of Different Nucleophiles,Producing Racemic 1-Substituted 3-Fluoro-2-Propanols. No By-Products Resulting From The Ring-Closure Reaction Have Been Detected,Confirming That Vicinal Fluoro Alcohols Are Not Substrates For Hhdh. Four Different 3-Fiuoro-2-Propanols Were Prepared Under Mild Reaction Conditions Starting From Epifluorohydrin. High Conversions Of 85-100% Were Reached Within 1-3 H And Depending On The Nucleophile Used Products Were Isolated In 31-92% Yields. (C) 2017 Elsevier Ltd. All Rights Reserved.
    DOI:10.1016/j.Tetlet.2017.12.054

    海关参考信息

    专利信息


    专利号:EP-1542943-A1
    优先权日:2002-08-06
    标 题:General synthesis of fluorine compounds

    专利号:WO-2004014820-A2
    优先权日:2002-08-06
    标 题 :General synthesis of fluorine compounds
    发明人:BRAUN MAX; BROSCH CARSTEN
    权利人:SOLVAY FLUOR & DERIVATE; BRAUN MAX; BROSCH CARSTEN

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    📌 第三方产品分析报告

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    合成参考文献


    摘要:U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals., NX#00320
    摘要:Haufe, G., Science of Synthesis, (2005) 34, 362.
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