反応式
[C:1]([CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])#[N:2].[ClH:9].C[O:11][C:12](C)(C)[CH3:13]>C(O)C>[ClH:9].[NH2:2][C:1]([O:11][CH2:12][CH3:13])=[CH:3][C:4]([O:6][CH2:7][CH3:8])=[O:5]参加物
5
実験手順
A solution of 226 g of ethyl cyanoacetate in 200 ml of absolute ethanol is saturated by introducing hydrochloric acid gas at 0°. The mixture is stirred at 0° overnight and then 1.5 l of tert.butyl methyl ether are added thereto. The ethyl β-amino-β-ethoxyacrylate hydrochloride which thereby precipitates is filtered off under suction, washed portionwise with 0.5 l of tert.butyl methyl ether and dried at 35° in vacuo. There is obtained ethyl β-amino-β-ethoxyacrylate hydrochloride, melting point 103°-104°.
後処理
- customThe ethyl β-amino-β-ethoxyacrylate hydrochloride which thereby precipitates
- filtrationis filtered off under suction
- washwashed portionwise with 0.5 l of tert.butyl methyl ether
- customdried at 35° in vacuo
出典と根拠
- ORDレコード
- ord-e155882b0fa7469fa0377d662f9667dc
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04549019
関連ノート
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