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HRID 26941생성일: 2026년 10월 24일

Hydrochloric Acid → 3-(2',4'-Difluoro-4-biphenylyl)-2-butenoic acid ethyl ester

https://huagongshe.com/ko/reaction/26941

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl trans-crotonateHCID 429065—
반응물Lithium ChlorideHCID 433294—
반응물2',4'-Difluoro-[1,1'-biphenyl]-4-amineHCID 2758266—
반응물Sodium NitriteHCID 23668193—
반응물2-Chloro-3-(2',4'-difluoro-4-biphenylyl)-2-butenoic acid ethyl esterHCID 53789753—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물3-(2',4'-Difluoro-4-biphenylyl)-2-butenoic acid ethyl esterHCID 54108058—

반응 단계

20.5 g. of 4-amino-2',4'-difluorobiphenyl are dissolved in a mixture of 25 ml. of 35% hydrochloric acid, 50 ml. of acetic acid and 120 ml. of water. The solution is cooled to 0° and 6.9 g. of NaNO2 are added in portions. Subsequently, a solution of 1.5 g. of Cu2Cl2, 0.9 g. of LiCl and 100 g. of crotonic acid ethyl ester in 900 ml. of acetone is added drop-wise at -10° to the stirred mixture under a N2 atmosphere. The mixture is stirred for 4 hours more at 0°-5° and for 14 hours at 20° and extracted with benzene. The extract is washed and evaporated to give 20 g. of crude 2-chloro-3-(2',4'-difluoro-4-biphenylyl)-2-butenoic acid ethyl ester. This is dissolved in 250 ml. of acetic acid to which 50 g. of zinc dust are added. The mixture is stirred for 3 hours at 20° and filtered. After the customary work up, 3-(2',4'-difluoro-4-biphenylyl)-2-butenoic acid ethyl ester, m.p. 54°-56°, is obtained from the filtrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04151302
출처 데이터셋uspto-grants-1979_04
ORD IDord-a770b524ce354360884f65f0ca48658c
출처 메모uspto-grants-1979_04