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 hours. A total of 93 ml of water was collected. The toluene residue was treated with 300 ml of ethanol and concentrated on the rotary evaportor. 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
- customslowly rose to 50° C
- temperatureAfter 0.5 hr the stirred mixture was heated
- temperatureto reflux
- customthe water was collected in a Dean-Stark trap for 48 hours
- customA total of 93 ml of water was collected
- additionThe toluene residue was treated with 300 ml of ethanol
- concentrationconcentrated on the rotary evaportor
- distillationThe residue was distilled
- customThe yield of product obtained
- custom145°/0.5 mm
出典と根拠
- ORDレコード
- ord-b804369893e54bd59770ee9a23839cc6
- 出典データセット
- uspto-grants-1988_02
- 特許番号
- US04727152
関連ノート
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