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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 918150생성일: 2026년 10월 26일

Hydrochloric Acid → Ethyl 3-(2-fluoro-4-biphenylyl)-2-butenoate

https://huagongshe.com/reaction/918150

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl bromoacetateHCID 7748—
반응물Phosphorus trichlorideHCID 24387—
반응물1-(2-Fluoro(1,1'-biphenyl)-4-yl)ethan-1-oneHCID 6451918—
촉매ZincHCID 23994—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매Ether tetrahydrofuranHCID 21868444—
생성물Ethyl 3-(2-fluoro-4-biphenylyl)-2-butenoateHCID 53797937—

반응 단계

42.8 gm (0.20 mol) of 4-acetyl-2-fluoro-biphenyl were added in small portions, while stirring, to a Reformatsky reagent prepared from 57.5 gm (0.88 mol) of zinc and 73.5 gm (0.44 mol) of bromoacetic acid ethyl ester in 500 ml of absolute ether/tetrahydrofuran (1:1), and the resulting mixture was refluxed for one hour. Then, 1 liter of water was added, the reaction mixture was acidified with dilute hydrochloric acid, and the organic layer was separated, extracted again with water and dried over sodium sulfate. The raw 3-(2-fluoro-4-biphenylyl)-3-hydroxy-butyric acid ethyl ester remaining after the solvent had been distilled off was refluxed in 330 ml of benzene with 45 gm (0.293 mol) of phosphorus trichloride for 10 minutes, whereupon the solvent was distilled off, water was added to the residue and the precipitated oil was taken up in ether. The ether solution was washed with water and an aqueous 5% sodium bicarbonate solution until neutral, dried, filtered through charcoal, and the solvent was distilled out of the filtrate. The residue, raw 3-(2-fluoro-4-biphenylyl)-2-butenoic acid ethyl ester (39.9 gm, 70% of theory), was used as a starting compound without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03969419
출처 데이터셋uspto-grants-1976_07
ORD IDord-cf92b890c2394305814db75427e6ccea
출처 메모uspto-grants-1976_07