1,1-Dimethylethyl 4-(hydroxyimino)-4-phenylbutylcarbamate → tert-butyl N-(4-amino-4-phenylbutyl)carbamate
反応式
O[N:2]=[C:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11]>C(O)C.[Pd]>[NH2:2][CH:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:11])[CH3:12]参加物
4
実験手順
1,1-Dimethylethyl 4-(hydroxyimino)-4-phenylbutylcarbamate (2.3 g, 8.3 mmol), in absolute ethanol was hydrogenated over 10% palladium on charcoal (0.5 g) at 5 bar pressure for 20 h. The mixture was then filtered and the filtrate concentrated to dryness to afford the title compound as a colourless oil (2.36 g).
後処理
- filtrationThe mixture was then filtered
- concentrationthe filtrate concentrated to dryness
出典と根拠
- ORDレコード
- ord-67fc204a87ee4cd9ade8e6b1f0e75ae7
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06743939B2
反応ノート
読み込み中…