反応式
[CH3:1][C:2]1[CH:10]=[C:9]([N+:11]([O-])=O)[C:8]([OH:14])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:15].[C:16](O)(=[O:18])[CH3:17]>[C].[Pd]>[CH3:1][C:2]1[CH:10]=[C:9]([NH:11][C:16](=[O:18])[CH3:17])[C:8]([OH:14])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:15]参加物
4
実験手順
Into a solution of 11.5 g of 4-methyl-6-nitro-7-hydroxy-1-indanone in 500 ml of acetic acid was added 1.5 g of 5% palladium carbon, then the mixture was subjected to a catalytic hydrogenation under an atmospheric pressure at a room temperature. The catalyst was removed by filtration and the solvent was removed by evaporation. The residue obtained was washed with ether and was recrystallized from methanol to obtain 6.34 g of 4-methyl-6-acetamido-7-hydroxy-1-indanone.
後処理
- customwas subjected to a catalytic hydrogenation under an atmospheric pressure at a room temperature
- customThe catalyst was removed by filtration
- customthe solvent was removed by evaporation
- customThe residue obtained
- washwas washed with ether
- customwas recrystallized from methanol
出典と根拠
- ORDレコード
- ord-acbcc05080a54311b75436cdf25ec350
- 出典データセット
- uspto-grants-1988_12
- 特許番号
- US04792628
関連ノート
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