CAS: 1864-94-4; Phenyl Formate

该化合物是一种有机化合物, 被归类为酯类, 由酚和丙酸形成, 青黄液体无色可用作糖, 水果味的特质. 苯甲酸酯在水中可中溶性,在有机溶剂中更易溶性,使其在各种应用中有用. 其化学配方是C8H8O2, 其沸点相对较低, 允许在需要挥发的工艺中使用. 该化合物以其再活动性为名, 特别是在酯化和转化反应中. 此外, 它可以用作溶剂, 并用于其他化学化合物的合成. 在处理苯丙胺时, 安全防范是必要的, 因为它可能会对皮肤和眼睛产生刺激, 其蒸气在吸入时可能有害. 总的来说, 苯乙基酸酯是多种化合物, 其应用在有机合成和食品工业中作为调料剂.

结构式图片

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上下游产品

formic acid tetraphenoxysilane phenyl chlorosulphinate formic acid silicic acid-anhydridedichloromethyl phenyl ether N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-formamideN-(5-phenyl-[1,3,4]oxadiazol-2-yl)-formamide 2-[(2,2-Dimethyl-propionyloxy)-phenoxy-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester 5-(2-formyl-6-methoxy-1,2,3,4,5,8-hexahydro-isoquinolin-1-ylmethyl)-2-methoxy-phenol

合成工艺路线路线简述

  • 合成目标产物 Phenyl Formate 主要起始原料 Formic Acid And Phenol
  • (文献来源)合成步骤主要原料 Formic Acid 和 Phenol
乙酸苯酯置于乙酸酐,四氯化钛,三乙胺体系中,用 二氯甲烷 用作溶剂,化学反应 5.5H,反应生成甲酸苯酯
参考文献:Ticl 4 / Et 3 N介导的乙酸酯和甲酸酯的缩合:直接获得β-烷氧基丙烯酸酯和β-芳氧基丙烯酸酯
标题:Ticl 4 / Et 3 N介导的乙酸酯和甲酸酯的缩合:直接获得β-烷氧基丙烯酸酯和β-芳氧基丙烯酸酯
摘要:提出了一种由ticl 4 / Et 3 N体系促进的乙酸酯和甲酸酯构建(e)-β-烷氧基-和(e)-β-芳氧基丙烯酸酯部分的方法.该反应与广泛的结构骨架相容,并通过不寻常的缩合途径而消失.考虑到所获得的结果,我们提出了一种可能的机制,其中涉及一种用于这种类型转化的双金属钛中间体.
Doi:10.1021/acs.Orglett.6B03233

海关参考信息

专利信息


专利号:US-9012625-B2
优先权日:2009-04-07
标 题 :Method for the synthesis of a trisaccharide
发明人:DÉKANY GYULA; Ã?GOSTON KÃ?ROLY; BAJZA ISTVAN; BOUTET JULIEN; BØJSTRUP MARIE; FANEFJORD METTE; PÉREZ FIGUEROA IGNACIO; HEDEROS MARKUS; HORVATH FERENC; KOVÃ?CS-PÉNZES PIROSKA; KRÖGER LARS; OLSSON JOHAN; RÖHRIG CHRISTOPH; SCHROVEN ANDREAS; VRASIDAS IOANNIS
权利人:DÉKANY GYULA; Ã?GOSTON KÃ?ROLY; BAJZA ISTVAN; BOUTET JULIEN; BØJSTRUP MARIE; FANEFJORD METTE; PÉREZ FIGUEROA IGNACIO; HEDEROS MARKUS; HORVATH FERENC; KOVÃ?CS-PÉNZES PIROSKA; KRÖGER LARS; OLSSON JOHAN; RÖHRIG CHRISTOPH; SCHROVEN ANDREAS; VRASIDAS IOANNIS; GLYCOM AS
摘要:The present invention relates to an improved synthesis of a trisaccharide of the formula (1), novel intermediates used in the synthesis and the preparation of the intermediates.

专利号:US-11542269-B2
优先权日:2018-01-03
标 题:Prins reaction and compounds useful in the synthesis of halichondrin macrolides and analogs thereof
发明人:CHOI HYEONG-WOOK; FANG FRANCIS G
权利人:EISAI R&D MAN CO LTD
摘要:The invention provides methods utilizing Prins reaction in the preparation of compounds that may be useful as intermediates in the synthesis of halichondrin macrolides and analogs thereof. The invention also provides compounds that may be useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.

专利号:US-5204456-A
优先权日:1986-04-08
标题:Derivatives of nucleosides and their use for the synthesis of oligonucleotides
发明人:MOLKO DIDIER; SCHULHOF JEAN-CLAUDE; TEOULE ROBERT
权利人:COMMISSARIAT ENERGIE ATOMIQUE
摘要:The invention relates to derivatives of nucleosides and their use for the synthesis of oligonucleotides. These derivatives are in accordance with the formula: (I) in which B represents a radical derived from guanine, cytosine or adenine, whose exocylic NH group is protected by the group with R1 representing a hydrogen atom or a alkyl radical and R2 a hydrogen atom, and alkyl radical, an alkoxy radical and optionally substituted aryloxy radical, R3 represents a hydrogen atom, the dimethoxytrityl radical or the radical R4 represents a hydrogen atom, the radical of formula: or a radical suitable for the synthesis of polynucelotides and R5 represents a hydrogen atom or the protected or unprotected hydroxyl OH radical.

专利号:US-10913749-B2
优先权日:2015-05-07
标 题 :Macrocyclization reactions and intermediates and other fragments useful in the synthesis of halichondrin macrolides
发明人:FANG FRANCIS G; KIM DAE-SHIK; CHOI HYEONG-WOOK; CHASE CHARLES E
权利人:EISAI R&D MAN CO LTD
摘要:The invention provides methods for the synthesis of a halichondrin macrolides through a macrocyclization strategy. The macrocyclization strategy of the present invention involves subjecting a non-macrocyclic intermediate to a carbon-carbon bond-forming reaction (e.g., an olefination reaction (e.g., Horner-Wadsworth-Emmons olefination), catalytic Ring-Closing Olefin Metathesis, or Nozaki-Hiyama-Kishi reaction) to afford a macrocyclic macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.

专利号:US-11136335-B2
优先权日:2016-06-30
标题:Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof
发明人:CHASE CHARLES E; CHOI HYEONG-WOOK; ENDO ATSUSHI; FANG FRANCIS G; KIM DAE-SHIK
权利人:EISAI R&D MAN CO LTD
摘要:The invention provides methods for the synthesis of a halichondrin macrolides or analogs thereof through a cyclization reaction strategy. The strategy of the present invention involves subjecting an intermediate to Prins reaction conditions to afford a macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides or analogs thereof and methods for preparing the same.

专利号:US-6512081-B1
优先权日:1997-07-21
标题:Synthesis of dithioester chain transfer agents and use of bis(thioacyl) disulfides or dithioesters as chain transfer agents
发明人:RIZZARDO ENZIO; THANG SAN HOA; MOAD GRAEME
权利人:E I DUPONT NEMOURS AND COMPANY; COMMW SCIENT IND RES ORG
摘要:This invention relates to the synthesis of dithiocarboxylic acid esters by reaction of bis(thioacyl) disulphides, thioacetals or vinylidane bis(thioether) with free-radicals (optionally in the presence of monomers). The invention also relates to processes for the synthesis of polymers utilising these dithioesters as polymerisation regulators (chain transfer agents) or to the use of bis(thioacyl) disulphides to generate dithioester chain transfer agents in situ.
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合成参考文献


摘要:Kwiecień, H., Science of Synthesis Knowledge Updates, (2018) 3, 134.
摘要:Gao, W.-C.; Tian, J., Science of Synthesis Knowledge Updates, (2020) 3, 242.
摘要:Neumann, H.; Schranck, J., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 2, 78.
摘要:Bertau, M.; Jeromin, G. E., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 1, 148.
摘要:Sokolovs, I.; Suna, E., Science of Synthesis: Hypervalent Halogens in Organic Synthesis, (2025) .
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