Sodium Hydroxide → L-Proline, 1-ethyl-5-oxo-

HRID 554109ノート

反応式

HRID 554109 の反応式
[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

  1. customThe ethanol was evaporated under vacuum
  2. extractionextracted with a 3:1 mixture of chloroform and isopropanol using a phase separator
  3. concentrationThe combined organic layers were concentrated to a pale yellow oil which
  4. customon drying in vacuo
  5. customcrystallized

出典と根拠

ORDレコード
ord-6213c73d62f64a3f85d00cb922231de7
出典データセット
uspto-grants-2011_11
特許番号
US08048907B2

反応ノート

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