Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26899Generated: October 25, 2026

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

https://huagongshe.com/reaction/26899

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151302
Source datasetuspto-grants-1979_04
ORD IDord-e10f69b05c2e4c25830c03c54053918b
Source noteuspto-grants-1979_04