反応式
[NH:1]1[CH2:8][S:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].CCOCC.[CH2:14]([O:21][C:22](Cl)=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>[OH-].[Na+]>[CH2:14]([O:21][C:22]([N:1]1[CH2:8][S:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
5
実験手順
In 94 ml of 2-N NaOH was dissolved 25 g of L-thioproline, and 20 ml of ether was added to the solution under agitation and ice-cooling. To this solution under agitation were added dropwise 38 ml of benzyloxycarbonyl chloride and 70 ml of 4-N NaOH at the same time in 30 minutes. The mixture was stirred for 2 hours at room temperature, washed with 100 ml of ether and treated with 6-N HCl to adjust pH to 2. The mixture was extracted with 200 ml and 100 ml of ethyl acetate and the ethyl acetate phase was washed 50 ml of water, dried over MgSO4 and filtered. The filtrate was concentrated until dryness under reduced pressure whereby an oily substance was obtained.
後処理
- additionwas added to the solution under agitation and ice-
- temperaturecooling
- washwashed with 100 ml of ether
- additiontreated with 6-N HCl
- extractionThe mixture was extracted with 200 ml and 100 ml of ethyl acetate
- washthe ethyl acetate phase was washed 50 ml of water
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationThe filtrate was concentrated until dryness under reduced pressure whereby an oily substance
- customwas obtained
出典と根拠
- ORDレコード
- ord-6a451b40f8a5463db5400fb49a3efa1b
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05411976
関連ノート
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