反応式
[CH2:1]([CH2:3][NH2:4])[OH:2].[C:5](O)(=[O:17])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>C1(C)C=CC=CC=1>[OH:2][CH2:1][CH2:3][NH:4][C:5](=[O:17])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]参加物
4
反応条件
- 温度
- 140 °C
実験手順
To a solution of 24 g (0.4 mole) ethanolamine in 100 ml toluene was added 40 g (0.2) lauric acid at 50° C. The mixture was refluxed for 6 hours. Toluene was gradually removed to increase the final pot temperature to 140° C. The distillate was collected in a Stark & Dean trap. The toluene was removed by vacuum stripping and the residue was crystallized from n-hexane. The title compound (44 g) thus obtained melted at 80°-84° C.
後処理
- temperatureThe mixture was refluxed for 6 hours
- customToluene was gradually removed
- distillationThe distillate was collected in a Stark & Dean trap
- customThe toluene was removed by vacuum stripping
- customthe residue was crystallized from n-hexane
出典と根拠
- ORDレコード
- ord-891d879642f2463097f63866a9287d86
- 出典データセット
- uspto-grants-1981_12
- 特許番号
- US04305868
関連ノート
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