反応式
[NH2:1][C:2]([CH3:7])([CH3:6])[CH2:3][CH2:4][OH:5].[CH:8](OCC)=[O:9]>>[CH:8]([NH:1][C:2]([CH3:7])([CH3:6])[CH2:3][CH2:4][OH:5])=[O:9]参加物
3
実験手順
3-Amino-3-methyl-1-butanol (20.60 g, 0.20 mol) was added to ethyl formate (29.60 g, 0.40 mol), and the resulting clear solution was heated to reflux under nitrogen for 2 hours, and then allowed to cool to room temperature. The ethyl formate and ethanol by-product were removed by rotary evaporation (35° C., 25 Torr). The resulting oil was dried under vacuum (25° C., 0.1 Torr) to yield 25.86 g (99%).
後処理
- temperaturethe resulting clear solution was heated
- temperatureto reflux under nitrogen for 2 hours
- customThe ethyl formate and ethanol by-product were removed by rotary evaporation (35° C., 25 Torr)
- customThe resulting oil was dried under vacuum (25° C., 0.1 Torr)
- customto yield 25.86 g (99%)
出典と根拠
- ORDレコード
- ord-a7ae87b463de419fa416f368a4dea82d
- 出典データセット
- uspto-grants-1991_01
- 特許番号
- US04988827
関連ノート
読み込み中…