反応式
[CH2:1]([N:3]1[C:12](=[O:13])[CH2:11][CH2:10][C@H:4]1[C:5]([O:7]CC)=[O:6])[CH3:2].[OH-].[Na+]>C(O)C>[CH2:1]([N:3]1[C:12](=[O:13])[CH2:11][CH2:10][C@H:4]1[C:5]([OH:7])=[O:6])[CH3:2]参加物
4
反応条件
- 温度
- 0 °C
実験手順
Ethyl 1-ethyl-5-oxoprolinate (1.33 g, 7.18 mmol) was dissolved in ethanol (10 ml) and cooled to 0° C. in an ice bath. To this was added 12.5M aqueous sodium hydroxide solution (1.72 ml, 21.53 mmol) and the mixture was stirred for ˜4 hours at 0° C. The ethanol was evaporated under vacuum and the aqueous residue was acidified with 2N aqueous hydrogen chloride to pH1. The volume of the aqueous phase was reduced to ˜3 ml under vacuum and then extracted with a 3:1 mixture of chloroform and isopropanol using a phase separator. The combined organic layers were concentrated to a pale yellow oil which on drying in vacuo crystallized to give 1-ethyl-5-oxoproline as a white solid (1.12 g).
後処理
- customThe ethanol was evaporated under vacuum
- extractionextracted with a 3:1 mixture of chloroform and isopropanol using a phase separator
- concentrationThe combined organic layers were concentrated to a pale yellow oil which
- customon drying in vacuo
- customcrystallized
出典と根拠
- ORDレコード
- ord-c7717be610cf4281a79b5b51e39f4c4b
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07718693B2
関連ノート
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