Methanol → 2,3-Dihydroxybutanedioic Acid
反応式
[CH:1]1[C:14]2[N:13]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][C:21]([CH2:24][CH:25]([O:31][CH2:32][CH3:33])[C:26]([O:28]CC)=[O:27])=[CH:20][CH:19]=3)[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[O:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH3:34][OH:35].[OH-:36].[Na+].[OH2:38]>>[CH:25]([OH:31])([C:26]([OH:28])=[O:27])[CH:24]([OH:38])[C:34]([OH:36])=[O:35].[CH:1]1[C:14]2[N:13]([CH2:15][CH2:16][O:17][C:18]3[CH:19]=[CH:20][C:21]([CH2:24][CH:25]([O:31][CH2:32][CH3:33])[C:26]([OH:28])=[O:27])=[CH:22][CH:23]=3)[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[O:6][C:5]=2[CH:4]=[CH:3][CH:2]=1参加物
実験手順
To a mixture of racemic ethyl 3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-ethoxypropionate of the formula (4) (45 g) obtained according to the procedure described in step (vi) above and methanol (225 ml) was added aqueous 10% sodium hydroxide solution (225 ml) slowly at room temperature over a period of 10–15 minutes. The reaction mixture was stirred at the same temperature for a period of 2–4 h. The progress of the reaction was monitored by TLC. After the complete hydrolysis of the compound of the formula (4), the reaction mass was diluted with water (225 ml) and washed with toluene to remove the impurities. The aqueous layer was acidified with dilute hydrochloric acid and extracted with toluene. The combined organic extracts were washed with water and concentrated under reduced pressure to half the volume and treated with activated charcoal. Filtration of the charcoal followed by concentration of toluene to ˜50 ml and precipitation with pet. ether afforded racemic acid of the formula (5) as an off-white to white solid, which was filtered and dried at room temperature (˜30° C.), (38–39 g 90–92%).
後処理
- customobtained
- washwashed with toluene
- customto remove the impurities
- extractionextracted with toluene
- washThe combined organic extracts were washed with water
- concentrationconcentrated under reduced pressure to half the volume
- additiontreated with activated charcoal
- filtrationFiltration of the charcoal
- customfollowed by concentration of toluene to ˜50 ml and precipitation with pet. ether
出典と根拠
- ORDレコード
- ord-781b3a880583435f8ba4096e01b5f891
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07223881B2
反応ノート
読み込み中…