反応式
[C:1]1(=[O:7])[CH:5]=[CH:4][C:3](=[O:6])[CH2:2]1.[CH3:8][C:9]([C:11]([CH3:13])=[CH2:12])=[CH2:10].C(C1C=C(O)C(C(C)(C)C)=CC=1O)(C)(C)C>C1C=CC=CC=1>[CH3:8][C:9]1[CH2:10][C@@H:5]2[C@H:4]([CH2:12][C:11]=1[CH3:13])[C:3](=[O:6])[CH2:2][C:1]2=[O:7]参加物
5
実験手順
A solution of 4-cyclopentene-1,3-dione (5.48g; 0.06 mole) and 2,3-dimethyl butadiene (10.4g; 0.127 mole) in dry benzene (20ml) were treated with a few crystals of 2,5-di-t-butyl hydroquinone and allowed to stand at ambient temperature for 4 days. After refluxing for 15 mins the mixture was cooled and the pale orange solid filtered. Recrystallisation from benzene, methanol afforded the title product as a white solid, m.p. 157°-158° C.
後処理
- temperatureAfter refluxing for 15 mins the mixture
- temperaturewas cooled
- filtrationthe pale orange solid filtered
- customRecrystallisation from benzene, methanol
出典と根拠
- ORDレコード
- ord-042502f6f7cc4aa09349c5beddc03164
- 出典データセット
- uspto-grants-1977_01
- 特許番号
- US04005219
関連ノート
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