Ethanol → HCID 21509235、化合物
反応式
[N+:1]([CH:4]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]1=[O:14])([O-:3])=[O:2].O.[CH2:16]([OH:18])[CH3:17]>>[CH2:16]([O:18][C:12]([CH:4]([N+:1]([O-:3])=[O:2])[C:5]([C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)=[O:14])=[O:13])[CH3:17]参加物
4
実験手順
2-Nitroindane-1,3-dione (20.5g; 0.107 moles) in ethanol (100 ml) was heated under reflux for 4 hours, cooled, poured into water (1 liter). allowed to stand overnight and filtered. The solid was extracted with 5% sodium bicarbonate solution (3 × 100 ml) and filtered. The insoluble solid was predominantly the ψ-ethyl ester, 3-ethoxy-3-nitromethylphthalide, contaminated with some α-ethyl ester. Acidification of the combined sodium bicarbonate filtrates, filtration and recrystallisation from ethanol gave the α-ethyl ester, 2-ethoxycarbonyl-ω-nitroacetophenone, m.p. 81°.
後処理
- temperatureunder reflux for 4 hours
- temperaturecooled
- filtrationfiltered
- extractionThe solid was extracted with 5% sodium bicarbonate solution (3 × 100 ml)
- filtrationfiltered
- filtrationAcidification of the combined sodium bicarbonate filtrates, filtration and recrystallisation from ethanol
出典と根拠
- ORDレコード
- ord-959f1727c99e470686ef06cc6689bea1
- 出典データセット
- uspto-grants-1976_09
- 特許番号
- US03983156
反応ノート
読み込み中…