Isoflavone → 2,3-dihydro-3-phenyl-4H-1-benzopyran-4-one
反応式
[O:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[C:3]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:2]1>C(O)(=O)C.[Pd]>[O:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[CH:3]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:2]1参加物
4
実験手順
Isoflavone (3.00 g) was dissolved in acetic acid (100 ml), and the solution hydrogenated at 50°-60° and 10.4-13.8 atm using 10% w/v palladium or carbon catalyst. The solution was filtered and evaporated, and the residue chromatographed on alumina, eluting with toluene. The product thus obtained gave, on recrystallisation from petroleum ether, (60°-80°) isoflavanone, 0.90 g., m.pt 73°-76°.
後処理
- customhydrogenated at 50°-60°
- filtrationThe solution was filtered
- customevaporated
- customthe residue chromatographed on alumina
- washeluting with toluene
- customThe product thus obtained
出典と根拠
- ORDレコード
- ord-cfc08dc7273e4acca11d397a90ffe462
- 出典データセット
- uspto-grants-1989_01
- 特許番号
- US04801593
反応ノート
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