反応式
[CH2:1]([O:8][C:9]([O:11]N1C(=O)CCC1=O)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:19][C@H:20]([C:24]([OH:26])=[O:25])[CH2:21][CH2:22][OH:23].C(=O)(O)[O-].[Na+]>O.CC(C)=O>[C:2]1([CH2:1][O:8][C:9]([NH:19][C@H:20]([C:24]([OH:26])=[O:25])[CH2:21][CH2:22][OH:23])=[O:11])[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
実験手順
N-(Benzyloxycarbonyloxy) succinimide (23.57 g., 94.58 mmol.) was added to a solution of L-homoserine (10.24 g., 85.98 mmol.) and sodium bicarbonate (7.95 g., 94.58 mmol., 1.1 eq.) in a mixture of water (100 ml.) and acetone (100 ml.). The mixture was stirred at room temperature overnight. The acetone was removed under reduced pressure (rotovap) and the aqueous solution was washed with methylene chloride (2×75 ml.). The aqueous layer was then acidified to pH 2 by addition of 6N hydrochloric acid and extracted with ethyl acetate (2×250 ml.). The combined ethyl acetate layers were washed with water (2×100 ml.) and brine, dried over sodium sulfate, filtered, concentrated and dried in vacuo to afford 19.54 g. of title product as a white solid. TLC (ethyl acetate:n-butanol:acetic acid:water; 2:1:1:1) Rf =0.74
後処理
- customThe acetone was removed under reduced pressure (rotovap)
- washthe aqueous solution was washed with methylene chloride (2×75 ml.)
- additionThe aqueous layer was then acidified to pH 2 by addition of 6N hydrochloric acid
- extractionextracted with ethyl acetate (2×250 ml.)
- washThe combined ethyl acetate layers were washed with water (2×100 ml.) and brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customdried in vacuo
- customto afford 19.54 g
出典と根拠
- ORDレコード
- ord-00c2290f10d84de2a8b56cbec5b23120
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05616775
関連ノート
読み込み中…