反応式
[CH:1]([C:3]1[C:4]2[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:5]=2[O:6][C:7]=1[CH3:8])=[O:2].[BH4-].[Na+].O>CO>[OH:2][CH2:1][C:3]1[C:4]2[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:5]=2[O:6][C:7]=1[CH3:8]参加物
5
実験手順
A mixture of 3-formyl-2-methyl-7-nitrobenzo[b]furan (1.83 g) and sodium borohydride (200 mg) in methanol (40 ml) was stirred at ambient temperature for 2 hours. The reaction mixture was poured into cold water. The separated oil was extracted with dichloromethane. The extract was washed with brine, dried and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give 3-hydroxymethyl-2-methyl-7-nitrobenzo[b]furan (1.38 g) as a solid.
後処理
- extractionThe separated oil was extracted with dichloromethane
- washThe extract was washed with brine
- customdried
- customevaporated in vacuo
- customThe residue was purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-37724ab1656547ecbe4ee241eb8c5182
- 出典データセット
- uspto-grants-1999_01
- 特許番号
- US05858995
関連ノート
読み込み中…