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HRID 26916作成日:2026年10月24日

Ether, ethyl ethynyl → 3-(2',4'-Difluoro-4-biphenylyl)-2-butenoic acid ethyl ester

https://huagongshe.com/ja/reaction/26916

反応式

関与物質

役割名称HCID仕込み量
反応物Ether, ethyl ethynylHCID 61239—
反応物1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-oneHCID 104542—
反応物HCID 178418443HCID 178418443—
反応物HCID 178467907HCID 178467907—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2',4'-Difluoro-4-biphenylyl)-2-butenoic acid ethyl esterHCID 54108058—

反応手順

A solution of 23.2 g. of 4-acetyl-2',4'-difluorobiphenyl in 50 ml. of THF and 50 ml. of ether is added slowly dropwise to a solution of 17.5 g. of ethoxyethinylmagnesium bromide in 200 ml. of ether, prepared by reacting ethoxyacetylene with ethyl magnesium bromide. The mixture is stirred for 1 hour at 20°. The reaction product is hydrolyzed with ice water/ammonium chloride and extracted with ether. The combined ether extracts are dried over MgSO4 and evaporated. Residual 1-ethoxy-3-(2',4'-difluoro-4-biphenylyl)-butyn-3-ol is dissolved in 200 ml. of 95% ethanol and 0.05 g. of solid CO2 is added to the solution and the mixture is left to stand for 12 hours at 20°. The customary work up gives 3-(2',4'-difluoro-4-biphenylyl)-2-butenoic acid ethyl ester, m.p. 54°-56°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151302
出典データセットuspto-grants-1979_04
ORD IDord-efe2eda672c94945a3f99d096be0d5a2
出典メモuspto-grants-1979_04