反応式
[OH:1][C@H:2]1[CH2:6][NH:5][C@@H:4]([C:7]([OH:9])=[O:8])[CH2:3]1.S(Cl)([Cl:12])=O.[CH3:14]O>>[ClH:12].[CH3:14][O:8][C:7](=[O:9])[C@H:4]1[CH2:3][C@@H:2]([OH:1])[CH2:6][NH:5]1参加物
4
反応条件
- 温度
- 0 °C
実験手順
A suspension of 65.0 g (0.50 mol) of cis4-hydroxy-D-proline in 1500 mL of methanol was cooled to 0° C. and 110 mL (179 g, 1.5 mol) of thionyl chloride was added dropwise at 0-5° C. The mixture was then allowed to warm to room temperature overnight. The volatiles were removed under reduced pressure and the residue was triturated with diethyl ether to afford 98.73 g of crude cis-4-hydroxy-D-proline methyl ester hydrochloride as a white solid.
後処理
- temperatureto warm to room temperature overnight
- customThe volatiles were removed under reduced pressure
- customthe residue was triturated with diethyl ether
出典と根拠
- ORDレコード
- ord-a21a8726fe624df980a5bf596cf50b51
- 出典データセット
- uspto-grants-2003_12
- 特許番号
- US06664400B2
関連ノート
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