反応式
[CH2:1]([NH:5][CH2:6][CH2:7][OH:8])[CH2:2][CH2:3][CH3:4].Cl[C:10]([O:12][CH2:13][CH3:14])=[O:11]>C(Cl)Cl>[OH:8][CH2:7][CH2:6][N:5]([CH2:1][CH2:2][CH2:3][CH3:4])[C:10](=[O:11])[O:12][CH2:13][CH3:14]参加物
4
実験手順
117.2 g of 2-(n-butylamino)ethanol and placed in 300 ml of methylene chloride. Then 54.3 g of ethyl chloroformate are allowed to drop in during 1 hour at 30°-35° C. with ice-cooling. After stirring for an additional 2 hours, the methylene chloride is evaporated and the residue is distilled to yield pure ethyl (2-hydroxyethyl)-n-butylcarbamate; b.p. 112° C./0.1 Torr.
後処理
- customto drop in during 1 hour at 30°-35° C. with ice-
- temperaturecooling
- customthe methylene chloride is evaporated
- distillationthe residue is distilled
出典と根拠
- ORDレコード
- ord-e4c48b7109eb4425bf1b91aa40ad4609
- 出典データセット
- uspto-grants-1986_08
- 特許番号
- US04607051
関連ノート
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