CAS: 123-62-6; Propionic Anhydride

该化合物是有机化合物,其特征为由丙酸衍生的碳氢化合物功能组,它看起来是无色的,可粉黄的黄色液体,有细微的气味.该化合物以反应性为名,特别是以其反应性为名,可以将丙烯基化合物组引入各种子体.丙烯基酐在诸如乙醚和氯仿等有机溶剂中可溶解,但不会因水的疏漏性而受水的侵扰.它有一个相对较低的沸点,使该物质挥发性.该物质主要用于推进剂的合成,并作为有机化学的试剂,用于培养酯类和亚胺.然而,必须小心地处理丙烯酸酐,因为它可能具有腐蚀性,并可能对皮肤,眼睛和呼吸系统造成刺激.在与该化学品合作时,适当的安全防范措施,包括使用个人防护设备,是不可或缺的.

结构式图片

欧盟法规

统一分类与标签REACH注册ECHA物质ECHA物质工作场所安全标识要求C&L通报REACH预注册废弃物危险特性清单

上下游产品

monoperoxyphthalic acid diethyl ether 3,4-hexanedione prop-1-en-1-one1-thiophen-2-yl-propan-1-one 2-(2-propionyloxy-benzyl)-benzofuran-3-carboxylic acid α-naphthyl propionate estradiol dipropionate

合成工艺路线路线简述

    丙酸置于chloro(1,5-Cyclooctadiene)Rhodium(I) Dimer,N-(2-Methylbenzoyl)-8-Aminoquinoline,Sodium Carbonate,N,N'-二环己基碳二亚胺体系中,用 甲苯 用作溶剂,化学反应 0.25H,以58%的收率获得丙酸酐
    参考文献:Rh催化脱羰基邻c-H烷基化(杂)芳烃与烷基羧酸的简便方法
    标题:Rh催化脱羰基邻c-H烷基化(杂)芳烃与烷基羧酸的简便方法
    摘要:已经开发了一种简便有效的方法,用于用市售羧酸对(杂)芳烃中的 C-H 键进行直接邻位烷基化反应.该策略是通过将羧酸原位转化为酸酐来启动的,酸酐无需分离,就经历了 Rh 催化的含有 8-氨基喹啉的芳基甲酰胺的直接脱羰基交叉偶联.该反应以高区域选择性进行,并表现出广泛的底物范围以及官能团耐受性.
    Doi:10.1039/d1Ra03992J

    海关参考信息

    专利信息


    专利号:US-2015284338-A1
    优先权日:2012-11-21
    标 题:Industrial process for the synthesis of pyrimidinyl-piperazine derivatives
    发明人:SZAVICSKÓ KRISZTINA; Domány György; Czibula László; Bartáné Szalai Gizella; Dobay László; WERKNÉ PAP ÉVA
    权利人:RICHTER GEDEON NYRT
    摘要:Our invention relates to trans-(4-{4-[2-(4-amino-cyclohexyl)-ethyl]-piperazin-1-yl}-5,6-dichloro-pyrimidin-2-yl)-methylamine dihydrochloride monohydrate, the process for the synthesis of this compound, the new (4,5-dichloro-6-piperazin-1-yl-pyirimidin-2-yl)-methylamine monohydrochlorid used as starting material in this synthesis, as well as the industrial process for the synthesis of trans-N-(4- {2-[4-(5,6-dichloro-2-methyl-amino-pyirimidin-4-yl-)piperazin-1-yl]-ethly}cyclohexyl-propionamide starting from trans-(4-{4-[2-(4-amino-cyclohexyl)-ethyl]-piperazin-1-yl}-5,6-dichloro-pyrimidin-2-yl)-methylamine dihydrochloride monohydrate.

    专利号:WO-2024084491-A1
    优先权日:2022-10-21
    标题:Process for synthesis of res metirom and its intermediates thereof
    发明人:MEHTA NILESH VIPINCHANDRA
    权利人:MEHTA NILESH VIPINCHANDRA
    摘要:The present invention discloses a process for synthesis of Res metirom and its intermediates thereof. More particularly, the invention discloses process for synthesis of a key intermediate, 6-(4-amino, 2,6-dichlorophenoxy)4- isopropylpyridazin-3(2H)-one, of Res metirom via novel intermediate compounds of formula A. Wherein, R is selected from methyl, ethyl and propyl.

    专利号:US-7692019-B2
    优先权日:2000-12-04
    标 题:Methods for the stereoselective synthesis of substituted piperidines
    发明人:AQUILA BRIAN M; BANNISTER THOMAS D; CUNY GREGORY D; HAUSKE JAMES R; HEFFERNAN MICHELE L R; HOEMANN MICHAEL Z; KESSLER DONALD W; SHAO LIMING; WU XINHE; XIE ROGER L
    权利人:SEPRACOR INC
    摘要:One aspect of the present invention relates to methods of synthesizing substituted piperidines. A second aspect of the present invention relates to stereoselective methods of synthesizing substituted piperidines. The methods of the present invention will find use in the synthesis of compounds useful for treatment of numerous ailments, conditions and diseases that afflict mammals, including but not limited to addiction and pain. An additional aspect of the present invention relates to the synthesis of combinatorial libraries of the substituted piperidines using the methods of the present invention. An additional aspect of the present invention relates to enantiomerically substituted pyrrolidines, piperidines, and azepines.

    专利号:US-3906004-A
    优先权日:1968-12-09
    标题 :Stereoselective synthesis of intermediate for preparation of meso-nordihydroguaiaretic acid
    发明人:PERRY CLARK WILLIAM
    权利人:HOFFMANN LA ROCHE
    摘要:This invention is directed to the stereoselective synthesis of the food additive meso-nordihydroguaiaretic acid from a protected ortho dihydroxy benzene and intermediates in this synthesis.

    专利号:US-9029547-B1
    优先权日:2013-12-07
    标 题 :Synthesis of 4-aryl 4-acyl piperidine, its salts and analogs using indium metal
    发明人:MAJEED MUHAMMED; RAMANUJAM RAJENDRAN; NAGABHUSHANAM KALYANAM
    权利人:MAJEED MUHAMMED; RAMANUJAM RAJENDRAN; NAGABHUSHANAM KALYANAM
    摘要:A novel process for the synthesis of 4-aryl 4-acyl piperidine derivatives using indium metal is described. Specifically, a novel process for the synthesis of 4-acetyl 4-phenyl piperidine and its salts using indium metal is described. This divisional application is specifically drawn to compounds 4-aryl 1,4-diacyl piperidine and 1,4 diacetyl 4-phenyl piperidine.

    专利号:US-9056868-B1
    优先权日:2012-09-13
    标题 :Three-step synthesis of CL-20
    发明人:WRIGHT MICHAEL E
    权利人:US NAVY
    摘要:Embodiments of the invention relate to the synthesis of CL-20 using only a three step synthesis and because of increased catalyst activity and lifetimes, a continuous flow process can be used with a tremendous reduction in total cost of producing CL-20.
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    山东省聊城市高新区九州街道长江路北燕山路西华建1街区小区8号商办楼8层8-0810室
    常规和库存产品*产品总量: 912

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    产品编号:A0851
    丙酸酐
    产品图片质量标准: 国标
    包装形式: 可定制包装
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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Isobenzofurans As Synthetic Intermediates: Synthesis And Biological Activity Of 8‐ Epi ‐(-)‐ajudazol B
    作者:Liam Adair,Ben A. Egan,Colin M. Pearson,Ricardo Lopez‐gonzalez,Michal Kuchar,Artemio Mendoza‐mendoza,Joëlle Prunet,Rodolfo Marquez |发布日期:2020.11.15
    摘要:The Step‐economic Convergent Total Synthesis Of 8‐epi‐(-)‐ajudazol B Has Been Achieved Taking Advantage Of Isobenzofuran As Synthetic Intermediates. This Approach Proves The Synthetic Utility Of Isobenzofurans As Reactive Intermediates And Provides A Fast And Efficient Way To Generate Ajudazol Analogues With Anti‐fungal Activity Through Minimal Manipulation.

    合成参考文献


    参考文献:10.1007/s00216-011-5224-8
    摘要:Bourgogne E, Mathy F, Boucaut D, Boekens H, Laprevote O. Simultaneous quantitation of histamine and its major metabolite 1-methylhistamine in brain dialysates by using precolumn derivatization prior to HILIC-MS/MS analysis. Analytical and Bioanalytical Chemistry. 2011 Jul 14;402(1):449–59. doi: 10.1007/s00216-011-5224-8.
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