(E)-3-(4-acetoxy-5-ethyl-3-methoxy-1-naphthyl)-2-methylpropenoic acid → E 5090
反応式
[C:1]([O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[CH2:15][CH3:16])[C:8](/[CH:17]=[C:18](\[CH3:22])/[C:19]([OH:21])=[O:20])=[CH:7][C:6]=1[O:23][CH3:24])(=[O:3])[CH3:2]>CC(C)=O>[C:1]([O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[CH2:15][CH3:16])[C:8](/[CH:17]=[C:18](/[CH3:22])\[C:19]([OH:21])=[O:20])=[CH:7][C:6]=1[O:23][CH3:24])(=[O:3])[CH3:2]参加物
3
実験手順
1.15 g of (E)-3-(4-acetoxy-5-ethyl-3-methoxy-1-naphthyl)-2-methylpropenoic acid was dissolved in 200 ml of acetone and irradiated with light from a high pressure mercury lamp through a Pyrex filter at room temperature for 3 hours. The reaction mixture was concentrated in vacuo and purified by silica gel column chromatography (3% methanol/chloroform) to obtain 470 mg of the titled compound as colorless crystals.
後処理
- customirradiated with light from a high pressure mercury lamp through a Pyrex
- filtrationfilter at room temperature for 3 hours