反応式
[OH:1][C:2]1[CH:3]=[C:4]([C:8]([CH3:17])([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]C)[CH3:9])[CH:5]=[CH:6][CH:7]=1.C(OC1C=CC=C(C(C)(C)C=CCCCCC)C=1)C1C=CC=CC=1>>[OH:1][C:2]1[CH:3]=[C:4]([C:8]([CH3:17])([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH3:9])[CH:5]=[CH:6][CH:7]=1参加物
3
実験手順
In like manner, 2-(3-hydroxyphenyl)-2-methylnonane is prepared in 82% (7.8 g.) yield from 13.0 g. (0.0406 mol.) of 1-benzyloxy-3-(1,1-dimethyl-oct-2-enyl)benzene. It is obtained as an oil having the characteristics:
後処理
- customyield from 13.0 g
- customIt is obtained as an oil
出典と根拠
- ORDレコード
- ord-3280d7f1a13e4d09bb779a3edf0c3d3e
- 出典データセット
- uspto-grants-1981_08
- 特許番号
- US04284829
関連ノート
読み込み中…