反応式
[CH3:1][O:2][C:3](=[O:13])[C@@H:4]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[NH2:5].[ClH:14].[OH-].[Na+]>O.COC(=O)[C@H](CC1C=CC=CC=1)N>[ClH:14].[CH3:1][O:2][C:3](=[O:13])[C@@H:4]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[NH2:5]参加物
6
反応条件
- 温度
- 2 °C
実験手順
An aqueous solution of 153.2 mmol of D-phenylalanine methyl ester and 4.6 mmol of L-phenylalanine methyl ester (D/L ratio=97.1/2.9) and 335 mmol of HCl in 400 ml of pure water was neutralized to pH 3 with a 20% NaOH aqueous solution and concentrated to a weight of 100 g by means of a rotary evaporator. The concentrate was cooled to about 2° C., and the precipitated crystals were collected by filtration by suction. There was obtained 120.7 mmol of D-phenylalanine methyl ester hydrochloride having an optical purity of 99.97% as measured by HPLC.
後処理
- concentrationconcentrated to a weight of 100 g by means of a rotary evaporator
- filtrationthe precipitated crystals were collected by filtration by suction
出典と根拠
- ORDレコード
- ord-a88b643517434cb992fa6cae6c5fd4a5
- 出典データセット
- uspto-grants-1999_12
- 特許番号
- US06008403
関連ノート
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