참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethyl bromoacetate | HCID 7748 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | 1-(2-Fluoro(1,1'-biphenyl)-4-yl)ethan-1-one | HCID 6451918 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ether tetrahydrofuran | HCID 21868444 | — |
| 생성물 | Ethyl 3-(2-fluoro-4-biphenylyl)-2-butenoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03969419 |
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| 출처 데이터셋 | uspto-grants-1976_07 |
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| ORD ID | ord-cf92b890c2394305814db75427e6ccea |
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| 출처 메모 | uspto-grants-1976_07 |
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