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HRID 26899作成日:2026年10月25日

Acetyl chloride → 3-(2',4'-Difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl ester

https://huagongshe.com/reaction/26899

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物Ethyl bromoacetateHCID 7748—
反応物1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-oneHCID 104542—
反応物2,4-Difluoro-1,1'-biphenylHCID 169974—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒BenzeneHCID 241—
溶媒TolueneHCID 1140—
生成物3-(2',4'-Difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl esterHCID 53834251—

反応手順

23.2 g. of 4-acetyl-2',4'-difluorobiphenyl, obtainable by reacting 2,4-difluorobiphenyl with acetyl chloride in the presence of AlCl3, and 11.1 ml. of ethyl bromoacetate are dissolved in a mixture of 75 ml. of benzene and 75 ml. of toluene. A 40 ml. portion of the resulting solution is added to 7 g. of zinc powder, previously washed successively with 1% hydrochloric acid, water and acetone and dried and the mixture is warmed to 70° with stirring and under a nitrogen atmosphere. After the reaction has begun, the remainder of the solution is added dropwise, the mixture is heated under reflux for one hour and cooled and 40 ml. of 20% sulfuric acid are added drop-wise in order to decompose the alcoholate Z--C(CH3) (OZnBr)--CH2 --COOC2H5 (Z is 2',4'-difluoro-4-biphenylyl). The organic phase is separated off and worked up in the customary manner to give 3-(2',4'-difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl ester, m.p. 96°-97° C.

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-e10f69b05c2e4c25830c03c54053918b
出典メモuspto-grants-1979_04