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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439030Generated: November 1, 2026

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

https://huagongshe.com/reaction/1439030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantEthyl bromoacetateHCID 7748—
Reactant1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-oneHCID 104542—
Reactant2,4-Difluoro-1,1'-biphenylHCID 169974—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
SolventTolueneHCID 1140—
Product3-(2',4'-Difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl esterHCID 53834251—

Reaction Steps

23.2 g. of 4-acetyl-2',4'-difluorobiphenyl, obtainable by reacting 2,4-difluorobiphenyl with actyl 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 actone 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 dropwise 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04057647
Source datasetuspto-grants-1977_11
ORD IDord-c985c20feb2c4e9c9187879b5b48680b
Source noteuspto-grants-1977_11