CAS: 2160-89-6; 1,1,1,3,3,3-Hexafluoropropan-2-Yl Acrylate

该化合物是氟丙烯酸化合物,其独特结构包括一个附于丙烯酯的六氟异丙基化合物组,以高热稳定性和低地表能源闻名,适于涂层,粘合剂和聚合物应用,需要增强化学抗药性和耐久性;氟芳烃原子的存在具有疏水特性,有助于其在水溶剂中的用途;此外,丙烯菊酯功能允许易于聚合,通过激进聚合技术形成各种聚合材料;其低挥发性和高再活性使其成为特殊聚合物和材料合成中有价值的中间体;应考虑安全因素,因为氟化合物可能对环境和健康造成危害;总体而言,1,1,1995,3,3-3,3-六氟丙基丙醇是一种具有重大工业用途的多用途化合物,特别是在开发先进材料方面.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

1,1,1,3',3',3'-hexafluoro-propanol acryloyl chloride 1,1,1,3,3,3-hexafluoropropan-2-yl (R)-3-hydroxy-2-methylene-3-phenylpropanoate 1,1,1,3,3,3-hexafluoropropan-2-yl (R)-3-cyclohexyl-3-hydroxy-2-methylenepropanoate methyl (S)-2-methanesulfonylamino-2-phenylacetate

合成工艺路线路线简述

    六氟异丙醇,丙烯酰氯置于三乙胺体系中,用 二氯甲烷 用作溶剂,化学反应生成1,1,1,3,3,3-六氟异丙基丙烯酸酯
    参考文献:铱(III)催化的β-三氟亚甲基烯酮羰基定向区域选择性邻-C(Sp2)-h烯化
    标题:铱(III)催化的β-三氟亚甲基烯酮羰基定向区域选择性邻-C(Sp2)-h烯化
    摘要:由于α,β-不饱和-β-三氟亚甲基酮的β位lumo能级低于其非氟化对应物,因此激活芳环的sp 2 C-H键存在挑战.在此,我们报道了氧化条件下铱( Iii )催化的β-三氟亚甲基烯酮羰基定向芳香族c(Sp 2 )-h与丙烯酸酯的区域选择性烯化反应.此外,还进行了与天然产物丙烯酸酯的偶联,放大和产品多样化.
    Doi:10.1039/d3Ob02024J

    海关参考信息

    专利信息


    专利号:US-10465033-B2
    优先权日:2016-11-10
    标题:One step synthesis of ultrahigh molecular weight block copolymers
    发明人:URBAN MAREK W
    权利人:UNIV CLEMSON; UNIV CLEMSON RES FOUNDATION
    摘要:Single-step synthesis processes for production of ultrahigh molecular weight block copolymers are described. The ultrahigh molecular weight copolymers can have a molecular weight of about 10 6 or greater and can be formed within a few hours in a surfactant-free environment. The formation process is controlled by initiator-starvation conditions in a sequential polymerization of monomers exhibiting different solubility in the solvent.

    专利号:US-9512250-B2
    优先权日:2012-02-23
    标 题 :Manganese catalyzed photopolymerization of fluorinated monomers
    发明人:ASANDEI ALEXANDRU D
    权利人:UNIV CONNECTICUT
    摘要:The disclosure discloses initiating systems for the radical polymerization of alkenes, and especially fluorine substituted alkenes. The polymerization is catalyzed by a metal carbonyl, preferably manganese carbonyl. The polymerization is initiated directly from alkyl halides at room temperature under visible white light. The polymers also allow the synthesis of block copolymers. The process comprises polymerizing at least one alkene monomer in the presence of a halide radical initiator, carbonyl catalyst and a solvent, under reaction conditions and for a time sufficient to polymerize the at least one alkene monomer to form a polymer. The present disclosure provides a method for living polymerization of alkene monomers which provides a high level of macromolecular control over the polymerization process and which leads to uniform and controllable polymeric products. This disclosure also provides a method for activating any halide (Cl, Br, I) chain ends of such polymers for the synthesis of block copolymerizations.

    专利号:EP-2647639-A1
    优先权日:2012-04-06
    标题:ß-boration of alkene and alkyne intermediates
    权利人:LEK PHARMACEUTICALS
    摘要:The present invention relates to the field of organic chemistry, and in particular to the preparation of β-borated compounds. These β-borated compounds can be used as intermediates in the synthesis of pharmaceutically active agents such as Sitagliptin.

    专利号:US-8053161-B2
    优先权日:2006-09-25
    标 题 :Resist composition, resin for use in the resist composition, compound for use in the synthesis of the resin, and pattern-forming method using the resist composition
    发明人:WADA KENJI; SAEGUSA HIROSHI
    权利人:FUJIFILM CORP
    摘要:A resist composition comprises: (A) a resin capable of increasing its solubility in an alkali developer by action of an acid; (B) a compound capable of generating an acid upon irradiation with actinic ray or radiation; (C) a resin having at least one of a fluorine atom and a silicon atom; and (D) a solvent, wherein the resin (C) has a degree of molecular weight dispersion of 1.3 or less and a weight average molecular weight of 1.0×10 4 or less.

    专利号:EP-2647640-A1
    优先权日:2012-04-06
    标 题:ß-boration of alkene and alkyne intermediates
    权利人:LEK PHARMACEUTICALS
    摘要:The present invention relates to the field of organic chemistry, and in particular to the preparation of β-borated compounds. These β-boated compounds can be used as intermediates in the synthesis of pharmaceutically active agents such as Sitagliptin.

    专利号:US-7902196-B2
    优先权日:2005-03-17
    标 题 :Synthesis of avrainvillamide, strephacidin B, and analogues thereof
    发明人:MYERS ANDREW G; HERZON SETH B; WULFF JEREMY EARLE; SIEGRIST ROMAIN; SVENDA JAKUB; ZAJAC MATTHEW ALLEN
    权利人:HARVARD COLLEGE
    摘要:The syntheses of the natural products, avrainvillamide and stephacidin B, are provided. The α,β-unsaturated nitrone functionality of avrainvillamide and its 3-alkylidene-3H-indole 1-oxide core is shown to covalently and reversibly bond to heteroatom-based nucleophiles. This capability may allow these molecules to bind active site nucleophiles and may provide the basis for designing potent and selective enzyme inhibitors. Both avrainvillamide and its dimer stephacidin B have been reported to exhibit antiproliferative activity, and avrainvillamide has been reported to exhibit antimicrobial activity against multi-drug resistant bacteria. Avrainvillamide has been found to target cytoskeleton-linking membrane protein (CLIMP-63) thereby preventing cells from undergoing mitosis. The invention provides syntheses of these natural products as well as analogs of these natural products and their functional cores. The compounds of the invention may be used in the treatment of diseases such as cancer, autoimmune diseases, and bacterial infection.
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    主要参考文献

    参考标题:α-Heteroarylation Of Thioethers Via Photoredox And Weak Brønsted Base Catalysis
    作者:Edwin Alfonzo,Sudhir M. Hande |发布日期:2021.8.6
    摘要:Thioethers To α-Thio Alkyl Radicals And Their Addition To N-Methoxyheteroarenium Salts For The Redox-Neutral Synthesis Of α-Heteroaromatic Thioethers. Studies Are Consistent With A Two-Step Activation Mechanism, Where Oxidation Of Thioethers To Sulfide Radical Cations By A Photoredox Catalyst Is Followed By α-C-H Deprotonation By A Weak Brønsted Base Catalyst To Afford α-Thio Alkyl Radicals. Further,

    合成参考文献


    摘要:Singh, R. P.; Deng, L., Science of Synthesis: Asymmetric Organocatalysis, (2012) 2, 50.
    摘要:Masson, G.; Zhu, J., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 739.
    摘要:Hatakeyama, S., Science of Synthesis: Asymmetric Organocatalysis, (2012) 1, 689.
    摘要:Jang, H. B.; Oh, J. S.; Song, C. E., Science of Synthesis: Asymmetric Organocatalysis, (2012) 2, 153.
    摘要:Hatakeyama, S., Science of Synthesis: Asymmetric Organocatalysis, (2012) 1, 673.
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