(3-Phenoxy-phenyl)-2-propyn-1-yl alcohol → 2,2-Dimethyl-3-(3-propoxy-3-oxo-1-propenyl)-cyclopropane-carboxylic acid
反応式
[CH3:1][C:2]1([CH3:16])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH2:10][CH2:11][CH3:12])=[O:8])[CH:3]1[C:13]([OH:15])=[O:14].O(C1C=C(C#CCO)C=CC=1)C1C=CC=CC=1>C(Cl)(Cl)Cl>[CH3:16][C:2]1([CH3:1])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH2:10][CH2:11][CH3:12])=[O:8])[CH:3]1[C:13]([OH:15])=[O:14].[CH3:16][C:2]1([CH3:1])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH2:10][CH2:11][CH3:12])=[O:8])[CH:3]1[C:13]([O-:15])=[O:14]参加物
5
反応物 2
生成物 2
試薬・触媒・溶媒 1
実験手順
Using the procedure of Example 9, (1R, cis, ΔZ) 2,2-dimethyl-3-(3-propoxy-3-oxo-1-propenyl)-cyclopropane-carboxylic acid and 1R (3-phenoxy-phenyl)-2-propyn-1-yl alcohol were reacted to obtain 1R (3-phenoxy-phenyl)-2-propyn-1-yl (1R, cis, ΔZ) 2,2-dimethyl-3-(3-propoxy-3-oxo-1-propenyl)-cyclopropane-carboxylate with a specific roation of [α]D20 =+48°±2° (c=1% in chloroform).
後処理
- customwere reacted
出典と根拠
- ORDレコード
- ord-dfd29c4a7898454f80fc2cf4d64f1736
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04833163
反応ノート
読み込み中…