Sodium Azide → Methyl 4-azido-3-hydroxybutyrate

HRID 362666

反応式

HRID 362666 の反応式
Cl[CH2:2][CH:3]([OH:9])[CH2:4][C:5]([O:7][CH3:8])=[O:6].[N-:10]=[N+:11]=[N-:12].[Na+]>CN(C)C1C=CN=CC=1.C(C(C)=O)C(C)C>[N:10]([CH2:2][CH:3]([OH:9])[CH2:4][C:5]([O:7][CH3:8])=[O:6])=[N+:11]=[N-:12]

参加物

5

実験手順

To a mixture of methyl 4-chloro-3-hydroxybutyrate (5 g, 33 mmol), and methyl isobutyl ketone (40 ml) are added sodium azide (2.3 g, 36 mmol) and 4-dimethylaminopyridine (403 mg, 3.3 mmol) and the mixture was refluxed under stirring for 11 hours. After cooling the salt was filtered off and the solvent was distilled off under vacuo and there was obtained methyl 4-azido-3-hydroxybutyrate (5.5 g) as a crude product. And followed by the same procedure as in example 1, there was obtained 4-hydroxy-2-pyrrolidone (2.3 g, 23 mmol, yield:70%). When the above reaction was carried out in the absence of 4-dimethylaminopyridine, it took more than 120 hours to detect the disappearance of the starting materials on gas chromatography.

後処理

  1. temperaturethe mixture was refluxed
  2. temperatureAfter cooling the salt
  3. filtrationwas filtered off
  4. distillationthe solvent was distilled off under vacuo

出典と根拠

ORDレコード
ord-e4bf2c4cf45f45a4a1954e8655437745
出典データセット
uspto-grants-1999_02
特許番号
US05869694

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