Ethyl orthoformate → HCID 10964674、化合物
反応式
[NH2:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4].[CH2:8](OC(OCC)OCC)[CH3:9]>C(O)C>[CH2:8]([O:6][C:5](=[O:7])[C@@H:2]([CH2:3][SH:4])[NH2:1])[CH3:9]参加物
反応条件
- 温度
- 70 °C
実験手順
To a suspension of D-cysteine 1.5 hydrate hydrochloride (Q-1, Scheme Q where RQ-1 and RQ-1 are equal to hydrogen, RQ-3 is hydrogen and stereochemistry is (S)) (5 g, 27.1 mmol) in absolute ethyl alcohol (50 mL) was added triethylorthoformate (13.5 mL, 81.2 mmol) at ambient temperature. A stream of anhydrous HCl gas was bubbled through the solution for 30 min. The stream of anhydrous HCl gas was maintained as the mixture heated to 70° C. for 2 h. The reaction mixture was concentrated in vacuo and the resulting residue triturated with diethyl ether to afford D-cysteine ethyl ester (4.43 g) as a white solid which was used without further purification. Physical data as follows: 1H NMR (300 MHz, D2O) 4.36 (1H), 4.27 (2H), 3.12 (2H), 1.25 (3H); MS (ESI+) for C5H11NO2S m/z 150.0 (M+H)+.
後処理
- customA stream of anhydrous HCl gas was bubbled through the solution for 30 min
- temperatureThe stream of anhydrous HCl gas was maintained as the mixture
- concentrationThe reaction mixture was concentrated in vacuo
- customthe resulting residue triturated with diethyl ether
出典と根拠
- ORDレコード
- ord-0148b6fb37474773ae8e6594902e5f86
- 出典データセット
- uspto-grants-2004_02
- 特許番号
- US06685617B1
反応ノート
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