Ethylamine → (CH3)3Coc(O)nhch2C(O)nhch2CH3
反応式
[CH2:1]([NH2:3])[CH3:2].CO[C:6](=[O:16])[CH2:7][NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10]>>[C:12]([O:11][C:9]([NH:8][CH2:7][C:6]([NH:3][CH2:1][CH3:2])=[O:16])=[O:10])([CH3:13])([CH3:14])[CH3:15]参加物
3
実験手順
Ethylamine (37 g, 0.82 mol) was condensed into a pressure vessel at 0° C. N-(tert-butoxycarbonyl)glycine methyl ester (50 mL, 0.34 mol) was added. The vessel was sealed and the mixture was stirred at room temperature overnight. The product mixture was concentrated under vacuum and the residue was passed through a pad of silica gel eluting with ethyl acetate. The solution was concentrated under vacuum to provide the title compound as a clear oil.
後処理
- customcondensed into a pressure vessel at 0° C
- customThe vessel was sealed
- concentrationThe product mixture was concentrated under vacuum
- concentrationThe solution was concentrated under vacuum
出典と根拠
- ORDレコード
- ord-b7f176b77d0a48b7bec71e30620c4bd3
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538112B2
反応ノート
読み込み中…