Sodium Hydroxide → trans-1-(3',4',5'-Trimethoxyphenyl)-6,7-methylenedioxy-4-tetralone-2-carboxylic acid
反応式
[C:1]([C:6]1(C(OCC)=O)[CH2:15][C:14](=[O:16])[C:13]2[C:8](=[CH:9][C:10]3[O:19][CH2:18][O:17][C:11]=3[CH:12]=2)[CH:7]1[C:20]1[CH:25]=[C:24]([O:26][CH3:27])[C:23]([O:28][CH3:29])=[C:22]([O:30][CH3:31])[CH:21]=1)([O:3]CC)=[O:2].[OH-].[Na+]>CO.O>[CH3:27][O:26][C:24]1[CH:25]=[C:20]([C@@H:7]2[C:8]3[C:13](=[CH:12][C:11]4[O:17][CH2:18][O:19][C:10]=4[CH:9]=3)[C:14](=[O:16])[CH2:15][C@H:6]2[C:1]([OH:3])=[O:2])[CH:21]=[C:22]([O:30][CH3:31])[C:23]=1[O:28][CH3:29]参加物
5
反応条件
- 温度
- 110 °C
実験手順
2,2-Dicarbethoxy-1-(3',4',5'-trimethoxyphenyl)-6,7-methylenedioxy-4-tetralone (XV; R2 = ethyl) (45 mg) was suspended in 10 ml of methanol. Aqueous NaOH (10 ml of 5%) was added and the mixture was refluxed for 3.5 hr. Then the mixture was cooled, diluted with water and washed one time with ether. The base layer was acidified to pH 2 with dilute sulfuric acid and extracted four times with chloroform. The organic layer was washed twice with water and once with saturated brine, and was dried over sodium sulfate. Filtration and evaporation gave a white solid which was heated briefly at 110° C. under nitrogen. Recrystallization of the white solid from methanol gave 24 mg (66%) of the title product, m.p. 221°-223° C.
後処理
- temperaturethe mixture was refluxed for 3.5 hr
- temperatureThen the mixture was cooled
- washwashed one time with ether
- extractionextracted four times with chloroform
- washThe organic layer was washed twice with water and once with saturated brine
- dry with materialwas dried over sodium sulfate
- filtrationFiltration and evaporation
- customgave a white solid which
- customRecrystallization of the white solid from methanol
出典と根拠
- ORDレコード
- ord-73cf8a7b75d04300914d80b5b2c7600f
- 出典データセット
- uspto-grants-1978_10
- 特許番号
- US04122092
反応ノート
読み込み中…