3-Chloro-2-methyl-1-propene → N-methallyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine
反応式
[CH2:1]([O:4][N:5]([C:16]([CH3:19])([CH3:18])[CH3:17])[C:6]([CH3:15])([CH3:14])[C:7]([NH:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH:2]=[CH2:3].[C:20](N(C(C)(C)C(NC(C)(C)C)=O)O)(C)(C)C.C(Cl)C(=C)C>>[CH2:1]([O:4][N:5]([C:16]([CH3:19])([CH3:18])[CH3:17])[C:6]([CH3:15])([CH3:14])[C:7]([NH:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[C:2](=[CH2:20])[CH3:3]参加物
4
反応物 3
生成物 1
実験手順
The compound is prepared in analogy to compound (204) from tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine and methallylchloride in 84% yield as colorless oil.
出典と根拠
- ORDレコード
- ord-379597fab6b9495dad5b9a0e2fffc288
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06518326B1
反応ノート
読み込み中…