反応式
[NH2:1][C@H:2]([C:4]([OH:6])=[O:5])[CH3:3].S(Cl)([Cl:9])=O.[CH2:11](O)[CH:12]([CH3:14])[CH3:13]>>[ClH:9].[CH2:11]([O:5][C:4](=[O:6])[C@H:2]([CH3:3])[NH2:1])[CH:12]([CH3:14])[CH3:13]参加物
4
実験手順
A mixture of 35.64 g (0.4 mol) of (D,L)-alanine (Aldrich) (or L-alanine (Aldrich)); 44 mL (0.6 mol) of thionyl chloride (Aldrich) and 200 mL of isobutanol was refluxed for 1.5 hours and the volatiles were removed completely on a rotavapor of 90° C. under reduced pressure to give (D,L)-alanine iso-butyl ester hydrochloride (or L-alanine iso-butyl ester hydrochloride), which was pure enough to be used for further transformations.
後処理
- customthe volatiles were removed completely on a rotavapor of 90° C. under reduced pressure
出典と根拠
- ORDレコード
- ord-67ada832f8c24662847c20f8da7631de
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06849650B2
関連ノート
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