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Succinic anhydride → (2S)-2-Carboxy-gamma-oxo-1-pyrrolidinebutanoic acid

HRID 65720
ノート
印刷プレビュー

反応式

HRID 65720 の反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH2:3][CH2:2]1.[NH:8]1[CH2:15][CH2:14][CH2:13][C@H:9]1[C:10]([OH:12])=[O:11]>C(O)(=O)C>[C:4]([CH2:3][CH2:2][C:1]([N:8]1[CH2:15][CH2:14][CH2:13][C@H:9]1[C:10]([OH:12])=[O:11])=[O:7])([OH:6])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7922Succinic anhydrideHCID 145742L-Proline

生成物 1

HCID 194156(2S)-2-Carboxy-gamma-oxo-1-pyrrolidinebutanoic acid

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

Succinic anhydride (67 mmoles, 6.7 g.) is dissolved in 100 ml. of hot glacial acetic acid and cooled to room temperature. To this, while stirring (67 mmoles, 7.7 g.) L-proline is added. After 20 hours at room temperature, the reaction mixture is concentrated to dryness in vacuo. The residue is extracted three times with hot ethyl acetate and cooled to room temperature. To the pooled extracts containing the 1-(3-carboxypropanoyl)-L-proline, dicyclohexylamine is added and crystals form which are recrystallized from hot isopropanol, yield 11.3 g. The dicyclohexylamine salt has m.p. (170°) 175°-177°.

後処理

  1. additionis added
  2. concentrationthe reaction mixture is concentrated to dryness in vacuo
  3. extractionThe residue is extracted three times with hot ethyl acetate
  4. additionTo the pooled extracts containing the 1-(3-carboxypropanoyl)-L-proline, dicyclohexylamine
  5. additionis added
  6. customcrystals form which are recrystallized from hot isopropanol, yield 11.3 g
  7. custom(170°) 175°-177°

出典と根拠

ORDレコード
ord-46e5eb741c8c431fa40ca721433c5e1f
出典データセット
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04128653

反応ノート

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