Methanol → Bmy 42393
反応式
[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]=1参加物
実験手順
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.
後処理
- 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)
出典と根拠
- ORDレコード
- ord-400836d2f6df463b9111887591735811
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05262540
反応ノート
読み込み中…