Ethyl chloroformate → N-(Ethoxycarbonyl)-D-norvaline
反応式
[NH2:1][C@@H:2]([C:6]([OH:8])=[O:7])[CH2:3][CH2:4][CH3:5].Cl[C:10]([O:12][CH2:13][CH3:14])=[O:11]>[OH-].[Na+]>[CH2:13]([O:12][C:10]([NH:1][C@@H:2]([C:6]([OH:8])=[O:7])[CH2:3][CH2:4][CH3:5])=[O:11])[CH3:14]参加物
4
実験手順
D-Norvaline (10.0 g, 85.3 mmol) was dissolved in aqueous sodium hydroxide (4M, 25 mL). Ethyl chloroformate (10.6 mL, 111 mmol) and aqueous sodium hydroxide (4M, 25 mL) was added over 15 min. at 0° C. The reaction mixture was warmed to room temperature and stirred at this temperature for 4 h. The reaction mixture was washed with diethyl ether three times and then acidified with aqueous hydrochloric acid (2M). The product was extracted with diethyl ether three times. The combined organic phases were dried over magnesium sulphate and concentrated in vacuo to yield the title compound in quantitative yield.
後処理
- washThe reaction mixture was washed with diethyl ether three times
- extractionThe product was extracted with diethyl ether three times
- dry with materialThe combined organic phases were dried over magnesium sulphate
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-ab13a9fc1221452db35569b17ff61465
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08158785B2
反応ノート
読み込み中…