反応式
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([SH:6])([CH3:5])[CH3:4].S(Cl)(Cl)=O.[CH3:14]O>>[NH2:1][C@@H:2]([C:3]([SH:6])([CH3:5])[CH3:4])[C:7]([O:9][CH3:14])=[O:8]参加物
4
実験手順
To a methanol (18 mL, 1.14 M) solution containing L-penicillamine (3.0 g, 20.11 mmol, 1.0 eq) was added thionyl chloride (1.5 mL, 20.7 mmol, 1.03 eq). The resulting mixture was heated to reflux for 18 hr and the solvent removed in vacuo. The resulting clear semi-solid was used in the next step without further purification. Isolated 3.28 g (20.1 mmol, 100% yield).
後処理
- temperatureThe resulting mixture was heated
- temperatureto reflux for 18 hr
- customthe solvent removed in vacuo
- customThe resulting clear semi-solid was used in the next step without further purification
- customIsolated 3.28 g (20.1 mmol, 100% yield)
出典と根拠
- ORDレコード
- ord-bd5e1b8e45af41ca92ca3e05f5afe5be
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07132443B2
関連ノート
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