Ethyl (2E)-3-ethoxy-2-butenoate → (E)-4-(3-Bromo-4-cyclohexyl-phenyl)-3-pentene-2-one
反応式
[Br:1][C:2]1[CH:3]=[C:4]([C:14](=O)[CH3:15])[CH:5]=[CH:6][C:7]=1[CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.C([O:19]/[C:20](/[CH3:27])=[CH:21]/C(OCC)=O)C>CO>[Br:1][C:2]1[CH:3]=[C:4](/[C:14](/[CH3:15])=[CH:21]/[C:20](=[O:19])[CH3:27])[CH:5]=[CH:6][C:7]=1[CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1参加物
4
実験手順
(E)-4-(3-Bromo-4-cyclohexyl-phenyl)-3-pentene-2-one was prepared analogous to Example 52, from 3'-bromo-4'-cyclohexylacetophenone (b.p. 135°-138°C at 0.15 mm Hg; nD20 = 1.5740) an ethyl (E)-3-ethoxy-crotonate with a yield of 69% of theory. B.p. 170°-175°C at 0.3 mm Hg; m.p. 52°-53°C (from methanol).
出典と根拠
- ORDレコード
- ord-1a14c392d3e74f2d8a6712e9a443216e
- 出典データセット
- uspto-grants-1976_04
- 特許番号
- US03950427
反応ノート
読み込み中…