Diketene → benzyl N-(2-acetoacetamidoethyl)carbamate
反応式
[NH2:1][CH2:2][CH2:3][NH:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:15]=[C:16]1[O:20][C:18](=[O:19])[CH2:17]1>CCOCC>[C:18]([NH:1][CH2:2][CH2:3][NH:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)(=[O:19])[CH2:17][C:16]([CH3:15])=[O:20]参加物
4
実験手順
A solution of benzyl N-(2-aminoethyl)carbamate (54 g, 0.276 mole) in ether (250 ml) and a solution of diketene (25.2 g, 0.30 mole) in ether (250 ml) were added simultaneously, dropwise, to ether (600 ml) while stirring and cooling over a 30 minute period. A white precipitate appeared. The solution was stirred 30 minutes longer, and then filtered. One recrystallization from water gave pure benzyl N-(2-acetoacetamidoethyl)carbamate (m.p.=116°-118° C.) at a yield of 90%.
後処理
- temperaturecooling over a 30 minute period
- filtrationfiltered
- customOne recrystallization from water
出典と根拠
- ORDレコード
- ord-9643bde6f84947c28080a65a151ef721
- 出典データセット
- uspto-grants-1981_01
- 特許番号
- US04247673
反応ノート
読み込み中…