돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26899생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/26899

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Ethyl bromoacetateHCID 7748—
반응물1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-oneHCID 104542—
반응물2,4-Difluoro-1,1'-biphenylHCID 169974—
반응물Aluminum(III) ChlorideHCID 6451240—
용매BenzeneHCID 241—
용매TolueneHCID 1140—
생성물3-(2',4'-Difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl esterHCID 53834251—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04151302
출처 데이터셋uspto-grants-1979_04
ORD IDord-e10f69b05c2e4c25830c03c54053918b
출처 메모uspto-grants-1979_04