반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[OH-].[K+].I[C:12]1[CH:17]=[CH:16][C:15]([CH:18]([CH3:22])[C:19]([OH:21])=[O:20])=[CH:14][CH:13]=1>O.[Cu]>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][C:12]1[CH:17]=[CH:16][C:15]([CH:18]([CH3:22])[C:19]([OH:21])=[O:20])=[CH:14][CH:13]=1참가 물질
반응 조건
- 온도
- 180 °C
실험 절차
2-Fluorophenol (2.35 g.) was fused with potassium hydroxide (1.7 g.) and a few drops of water by heating to 180° C. 2-(4-Iodophenyl)propionic acid (2.76 g.) and copper powder (0.1 g.) were then added and the melt ws heated at 160°-170° C. for 1 hour. The cooled solid was partitioned with methylene chloride (50 ml.) and 2.5N sodium hydroxide (50 ml.). The aqueous layer was acidified with hydrochloric acid, the resulting gum was extracted into ether, and the ether extract was extracted with saturated potassium carbonate solution. This aqueous extract was acidified with hydrochloric acid and the product isolated in ether. After evaporation the resulting solid was purified by preparative layer chromatography using 5% acetic acid/petroleum ether b.p. 62°-68° C. and eluting with ethyl acetate. Recrystallization from petroleum ether b.p. 62°-68° C. gave 2-[4-(2-fluorophenoxy)phenyl]propionic acid, m.p. 106°-108° C.
후처리
- temperaturethe melt ws heated at 160°-170° C. for 1 hour
- customThe cooled solid was partitioned with methylene chloride (50 ml.) and 2.5N sodium hydroxide (50 ml.)
- extractionthe resulting gum was extracted into ether
- extractionthe ether extract
- extractionwas extracted with saturated potassium carbonate solution
- extractionThis aqueous extract
- customthe product isolated in ether
- customAfter evaporation the resulting solid
- customwas purified by preparative layer chromatography
- washeluting with ethyl acetate
- customRecrystallization from petroleum ether b.p. 62°-68° C.
출처 및 근거
- ORD 기록
- ord-a480ab6c73eb43689a2bfa1d299ef1ed
- 출처 데이터셋
- uspto-grants-1978_12
- 특허 번호
- US04128573
연결된 노트
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