N-(4-Chlorophenyl)acetamide → 2-[4-(4-Chloroanilino)-phenyl]propionic acid
반응식
I[C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:13])[C:9]([O:11]C)=[O:10])=[CH:4][CH:3]=1.CC([NH:17][C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=1)=O.C(=O)([O-])[O-].[K+].[K+]>[Cu]>[Cl:24][C:21]1[CH:22]=[CH:23][C:18]([NH:17][C:2]2[CH:7]=[CH:6][C:5]([CH:8]([CH3:13])[C:9]([OH:11])=[O:10])=[CH:4][CH:3]=2)=[CH:19][CH:20]=1참가 물질
실험 절차
Methyl 2-(4-iodophenyl)propionate (2 g.), acet-p-chloroanilide (1.17 g.), potassium carbonate (0.62 g.) and copper powder (0.1 g.) were heated at 165°C. for 7.5 hours. The cooled solid was triturated with methylene chloride, filtered, and the filtrate evaporated to dryness. The residue was refluxed for 1.5 hours with ethanol (7 ml.) and 2.5N sodium hydroxide (14 ml.); ethanol was distilled in vacuo and the residue diluted with water, washed with ether and acidified with dilute hydrochloric acid. The resulting oil was isolated in ether and evaporated to dryness. The resulting gum was purified by preparative layer chromatography using 5% acetic acid/petroleum ether b.p. 62°-68°C. and eluting with ethyl acetate; recrystallization from benzene/petroleum ether b.p. 62°-68°C. and from petroleum ether b.p. 80°-100°C. gave 2-[4-(4-chloroanilino)-phenyl]propionic acid, m.p. 106-109°C.
후처리
- customThe cooled solid was triturated with methylene chloride
- filtrationfiltered
- customthe filtrate evaporated to dryness
- temperatureThe residue was refluxed for 1.5 hours with ethanol (7 ml.) and 2.5N sodium hydroxide (14 ml.)
- distillationethanol was distilled in vacuo
- additionthe residue diluted with water
- washwashed with ether
- customThe resulting oil was isolated in ether
- customevaporated to dryness
- customThe resulting gum was purified by preparative layer chromatography
- washeluting with ethyl acetate
- customrecrystallization from benzene/petroleum ether b.p. 62°-68°C.
출처 및 근거
- ORD 기록
- ord-1f49bad261de4cf89ce7a4d1bf627ad7
- 출처 데이터셋
- uspto-grants-1976_09
- 특허 번호
- US03981905
반응 노트
불러오는 중…