Methylamine → (S)-N-Methylhydroxysuccinimide

HRID 247261

反応式

HRID 247261 の反応式
[C:1]([OH:9])(=O)[C@H:2]([CH2:4][C:5](O)=[O:6])[OH:3].[CH3:10][NH2:11]>C1(C)C=CC=CC=1>[OH:3][C@H:2]1[CH2:4][C:5](=[O:6])[N:11]([CH3:10])[C:1]1=[O:9]

参加物

4

実験手順

To a stirred solution of 134 g (1 mole) of (S)-malic acid in 700 ml of toluene was added 97 ml of 40% aqueous methylamine. The temperature slowly rose to 50° C. After 0.5 hr the stirred mixture was heated to reflux and the water was collected in a Dean-Stark trap for 48 hr. A total of 93 ml of water was collected. The toluene residue was treated with 300 ml of ethanol and concentrated on the rotary evaporator. The residue was distilled. The yield of product obtained was 101 g (78%), b.p. 140°/2 mm; 145°/0.5 mm.

後処理

  1. customslowly rose to 50° C
  2. temperatureAfter 0.5 hr the stirred mixture was heated
  3. temperatureto reflux
  4. customthe water was collected in a Dean-Stark trap for 48 hr
  5. customA total of 93 ml of water was collected
  6. additionThe toluene residue was treated with 300 ml of ethanol
  7. concentrationconcentrated on the rotary evaporator
  8. distillationThe residue was distilled
  9. customThe yield of product obtained
  10. custom145°/0.5 mm

出典と根拠

ORDレコード
ord-512c2949d3fb413fab290e42eb1b5ccc
出典データセット
uspto-grants-1987_11
特許番号
US04705853

関連ノート

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