Ethyl orthoformate → HCID 10964674、化合物

HRID 2119291ノート

反応式

HRID 2119291 の反応式
[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

4

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

  1. customA stream of anhydrous HCl gas was bubbled through the solution for 30 min
  2. temperatureThe stream of anhydrous HCl gas was maintained as the mixture
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. 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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