Methanol → Bmy 42393
반응식
[C:1]1([C:7]2[N:8]=[C:9]([CH2:18][CH2:19][C:20]3[CH:21]=[C:22]([CH:29]=[CH:30][CH:31]=3)[O:23][CH2:24][C:25]([O:27]C)=[O:26])[O:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].CO>Cl>[C:1]1([C:7]2[N:8]=[C:9]([CH2:18][CH2:19][C:20]3[CH:21]=[C:22]([CH:29]=[CH:30][CH:31]=3)[O:23][CH2:24][C:25]([OH:27])=[O:26])[O:10][C:11]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
실험 절차
A mixture of methyl 2-[3-[2-(4,5-diphenyl-2-oxazolyl)ethyl]phenoxy]acetate (2.25 g, 5.5 mmol), 3N sodium hydroxide solution (5.5 mL) and methanol (50 mL) was heated to reflux on a steam bath. After 5 minutes, the mixture was cooled, the methanol evaporated and the residue diluted with water. Warming provided a solution which was diluted with 1N hydrochloric acid solution to pH 3 to give an oily precipitate. The mixture was extracted with CH2Cl2 and the organic extracts washed twice with water and once with saturated sodium chloride solution. Concentration, after drying over sodium sulfate, left a pale yellow solid which was recrystallized twice from a mixture of hexanes and CH2Cl2 (2:1) to give 2-[3-[2-(4,5-diphenyl-2-oxazolyl)-ethyl]phenoxy]acetic acid (1.74 g, 80%), m.p. 153.3°-154.5° C.
후처리
- temperaturewas heated
- temperatureto reflux on a steam bath
- temperaturethe mixture was cooled
- customthe methanol evaporated
- additionthe residue diluted with water
- temperatureWarming
- customprovided a solution which
- customto give an oily precipitate
- extractionThe mixture was extracted with CH2Cl2
- washthe organic extracts washed twice with water and once with saturated sodium chloride solution
- concentrationConcentration
- dry with materialafter drying over sodium sulfate
- waitleft a pale yellow solid which
- customwas recrystallized twice from a mixture of hexanes and CH2Cl2 (2:1)
출처 및 근거
- ORD 기록
- ord-400836d2f6df463b9111887591735811
- 출처 데이터셋
- uspto-grants-1993_11
- 특허 번호
- US05262540
반응 노트
불러오는 중…