CAS: 422-05-9; 2,2,3,3,3-Pentafluoro-1-Propanol

该化合物是一种含氟酒精,其独特的结构特征是:一种含五氟原子的丙醇脊柱,与碳链相连;该化合物在室温下是一种无色液体,由于氢氧(OH)组的存在,其极地性高,氢结扎能力强;其含氟性质具有很强的热稳定性和抗氧化性,使其在各种应用中,包括作为一种溶剂和氟化合物合成中发挥作用;多种氟基质的存在,增强了其疏水性,从而影响其在生物系统和环境相互作用中的行为;此外,2,2,3,3,3,4-全氟丙醇的挥发性较低,有助于其在专门化学工艺中的用途;在处理该物质时,安全考虑十分重要,因为吸入或摄入该物质可能会对健康造成危害,因此应当采取适当的预防措施,以尽量减少接触.

结构式图片

相似化合物

422-64-0 426-65-3 76-37-9

欧盟法规

REACH注册ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

ethylmagnesium iodide diethyl ether 2,2,3,3,3-Pentafluoro-propionaldehyde isopropylmagnesium bromide2,2,3,3,3-pentafluoropropyl acrylate 2-((2,2,3,3,3-pentafluoropropyloxy)methyl)oxirane 2,2,3,3,3-pentafluoropropyl triflate (2,2,3,3,3-Pentafluor-propyloxy)-triphenyl-silan

合成工艺路线路线简述

  • 合成目标产物 Pentafluoro-1-Propanol 主要起始原料 Perfluoropropionic Acid
  • (文献来源)合成步骤主要原料 Perfluoropropionic Acid
五氟丙胺置于lialh4体系中,用 二丁醚 作为反应溶剂,以81%的收率获得产物2,2,3,3,3-五氟-1-丙醇
参考文献:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: F: Perfhalorg.7,1,Page 1-84
标题:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: F: Perfhalorg.7,1,Page 1-84

海关参考信息

专利信息


专利号:US-6909010-B2
优先权日:2001-04-11
标题:Facile synthesis of symmetric esters of alkylenebisphosphonic acids
发明人:HERLINGER ALBERT W; STEPINSKI DOMINIQUE C
权利人:UNIV LOYOLA CHICAGO
摘要:A facile synthesis of symmetric esters of C 1 -C 10 alkylenebisphopsphonic acids is disclosed in which a C 1 -C 10 alkylenebis(phosphonic dichloride) is reacted with an alcohol in the presence of a catalytic amount of 1H-tetrazole and a base in an aprotic solvent to form a first reaction mixture. The first reaction mixture is maintained for a time period sufficient to form a C 1 -C 10 alkylenebis(chloro ester phosphonate) that is reacted under basic conditions with an excess of a hydroxylated compound to form a second reaction mixture that is itself maintained for a time period sufficient to form a C 1 -C 10 alkylenebis(ester phosphonate) partial ester, homoleptic tetraester or mixed tetraester. The material so formed can be recovered or used as is.

专利号:US-2008280855-A1
优先权日:2005-06-22
标 题 :Process For the Production of Intermediates For the Preparation of Tricyclic Benzimidazoles
发明人:CHIESA MARIA VITTORIA; PALMER ANDREAS; BUHR WILM; ZIMMERMANN PETER JAN; BREHM CHRISTOF; SIMON WOLFGANG-ALEXANDER; POSTIUS STEFAN; KROMER WOLFGANG; ZANOTTI-GEROSA ANTONIO
权利人:NYCOMED GMBH
摘要:The invention relates to a process for the synthesis of compounds of the formula 1-a and compounds of the formula 1-b. n n n n n n n n n n The compounds of the formula 1-a and the compounds of the formula 1-b, in which the substituents R1, R2, R3, and Ar have the meanings indicated in the description, are valuable intermediates for the preparation of pharmaceutically active compounds.

专利号:US-4273947-A
优先权日:1979-01-31
标 题:Hydrogenation of fluorine-containing carboxylic acids
发明人:NOVOTNY MIROSLAV
权利人:ALLIED CHEM
摘要:A process is described for the heterogeneous hydrogenation of fluorine-containing alkyl, cycloalkyl, and benzene carboxylic acids to the corresponding primary alcohols. The hydrogenation can be carried out in the liquid or vapor phase in the presence of a solid rhodium or iridium catalyst, employed as the metal, metallic oxide, or mixture thereof. In the liquid phase, the hydrogenation can be carried out batchwise under mild conditions of temperature and pressure, preferably at about 50°-150° C. and about 5-15 atmospheres, in an atmosphere containing hydrogen gas. A preferred embodiment is the hydrogenation of trifluoroacetic acid in the liquid phase to 2,2,2-trifluoroethanol, said alcohol being useful as an intermediate in the synthesis of the anesthetic, isoflurane, CF 3 CHClOCHF 2 .

专利号:US-2013197280-A1
优先权日:2009-12-29
标 题:Synthesis of fluorinated olefins from fluorinated alcohols
发明人:STEPANOV ANDREI ALEKSANDROVICH; CHERSTKOV VICTOR FILIPPOVICH; NAPPA MARIO JOSEPH
权利人:STEPANOV ANDREI ALEKSANDROVICH; CHERSTKOV VICTOR FILIPPOVICH; NAPPA MARIO JOSEPH; DU PONT
摘要:Disclosed is a process for producing a hydrofluoroalkene, R f CFâ•?CH 2 comprising contacting a hydrofluoroalkanol of structure R f CF 2 CH 2 OH, with a lewis acid to produce a mixture, diluting said mixture with a solvent to produce a solvent mixture, contacting the solvent mixture with a reactive metal, heating the solvent mixture and reactive metal for a sufficient amount of time to produce a hydrofluoroalkene, and condensing and collecting the volatile products comprising the hydrofluoroalkene, wherein R f is F, or a fluorine-substituted alkyl group.

专利号:US-4255594-A
优先权日:1979-09-18
标题 :Hydrogenation of halogen-containing carboxylic anhydrides
发明人:NOVOTNY MIROSLAV
权利人:ALLIED CHEM
摘要:A process is described for the heterogeneous hydrogenation of haloalkyl, halocycloalkyl or haloaryl carboxylic anhydrides to the corresponding primary alcohols. In the haloalkyl or halocycloalkyl carboxylic anhydrides at least one halogen is in the alpha-position relative to the carboxylic anhydride grouping. The hydrogenation can be carried out in the liquid or vapor phase in the presence of a supported or unsupported catalyst comprising a member of the group consisting of rhodium, iridium, metal oxides thereof, or mixtures thereof. In the liquid phase, the hydrogenation can be carried out batchwise under mild conditions of temperature and pressure, preferably at about 50°-150° C. and about 5-15 atmospheres, in an atmosphere containing hydrogen gas. A preferred embodiment is the hydrogenation of trifluoroacetic anhydride in the liquid phase to 2,2,2-trifluoroethanol, said alcohol being useful as an intermediate in the synthesis of the anesthetic, isoflurane, CF 3 CHClOCHF 2 .

专利号:US-2012095211-A1
优先权日:2010-09-22
标 题 :Substituted proline inhibitors of hepatitis c virus replication
发明人:BUCKMAN BRAD; NICHOLAS JOHN B; SEREBRYANY VLADIMIR; SEIWERT SCOTT D
权利人:BUCKMAN BRAD; NICHOLAS JOHN B; SEREBRYANY VLADIMIR; SEIWERT SCOTT D; INTERMUNE INC
摘要:The embodiments provide compounds of the general Formulae I, Ia, II, IIa, III, IIIa, IIIb, IV, IVa, IVb, V, Va, Vb, VI, VIa, VIb, and VIc, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition. The embodiments also provide methods for the synthesis of subject compounds and intermediates in the synthetic methods.
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[参考文献]: Callie A Cole, Et Al. Anionic Derivatives Of Uracil: Fragmentation And Reactivity. Phys Chem Chem Phys. 2014 Sep 7;16(33):17835-44.
[参考文献]: Dilek Battal, Et Al. Urine Mescaline Screening With A Biochip Array Immunoassay And Quantification By Gas Chromatography-Mass Spectrometry. Ther Drug Monit. 2015 Dec;37(6):805-11.
[参考文献]: M Usami, Et Al. [参考文献]: Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 2000:(118):45-9.
[参考文献]: Mitsue Sano, Et Al. Simultaneous Detection Of Stable Isotope-Labeled And Unlabeled L-Tryptophan And Of Its Main Metabolites, L-Kynurenine, Serotonin And Quinolinic Acid, By Gas Chromatography/negative Ion Chemical Ionization Mass Spectrometry. J Mass Spectrom. 2014 Feb;49(2):128-35.
[参考文献]: Patrick S Cardona, Et Al. Simultaneous Analyses Of Cocaine, Cocaethylene, And Their Possible Metabolic And Pyrolytic Products. Forensic Sci Int. 2006 Feb 10;157(1):46-56.

合成参考文献


摘要:Journal of Occupational Medicine., 4(262), 1962
摘要:S125 | FLUOROIONS | Fluorinated Ionic Liquids Suspect List | DOI:10.5281/zenodo.15348301.
摘要:S124 | IONICLIQUIDS | Ionic Liquids Suspect List | DOI:10.5281/zenodo.15348268.
摘要:Hou, W.; Yang, G.; Xu, H., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 185.
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