3,4,5-Trimethylphenol → 2-(3,4,5-trimethylphenoxy)-3-methoxy-N-(4-methylpent-2-yn-4-yl)propionamide
反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:10])[CH:5]=[C:6]([CH3:9])[C:7]=1[CH3:8].Br[CH:12]([CH2:22][O:23][CH3:24])[C:13]([NH:15][C:16]([CH3:21])([CH3:20])[C:17]#[C:18][CH3:19])=[O:14]>>[CH3:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([CH3:9])[C:7]=1[CH3:8])[O:10][CH:12]([CH2:22][O:23][CH3:24])[C:13]([NH:15][C:16]([CH3:21])([CH3:20])[C:17]#[C:18][CH3:19])=[O:14]参加物
3
実験手順
In a similar procedure to Example 3 Stage 2, 3,4,5-trimethylphenol was reacted with 2-bromo-N-(4-methylpent-2-yn-4-yl) 3-methoxypropionamide to give the title product as a colourless gum. 1H NMR (CDCl3) δ: 1.61(6H, s); 1.80(3H, s); 2.11(3H, s); 2.26(6H, s); 3.40(3H, s); 3.82(2H, m); 4.53(1H, t); 6.62(2H, s); 6.66(1H, s).
出典と根拠
- ORDレコード
- ord-685254be2e7443958f769769761593cb
- 出典データセット
- uspto-grants-2007_09