反応式
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([CH3:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].C([O-])([O-])=O.[K+].[K+].[Br:18][CH2:19][CH2:20][CH2:21]Br>C(#N)C>[Br:18][CH2:19][CH2:20][CH2:21][O:11][C:3]1[CH:4]=[CH:5][C:6]([C:8](=[O:9])[CH3:10])=[CH:7][C:2]=1[CH3:1]参加物
実験手順
A mixture of 4-hydroxy-3-methylacetophenone (14.5 g, 96 mmol), K2CO3 (17.5 g, 144 mmol), and 1,3-dibromopropane (30 g, 144 mmol) in acetonitrile (400 ml) was heated at reflux for 6 hours. At the end of the reaction, the solvent was removed on a rotary evaporator, and the crude solid was extracted into dichloromethane (750 ml). The insoluble inorganics were filtered off. The dichloromethane solution was concentrated again to a crude oil (34.5 g). Purification was effected by flash chromatography over a silica gel column (SiO2, 150 g; eluted with 7:3 hexane:dichloromethane, 2 l; and dichloromethane 2 l). The material thus purified weighed 14.6 g (56%) and was recrystallized from ethanol. Recrystallization again from ethanol gave analytically pure 1-[4-(3-bromopropoxy)-3-methylphenyl]ethanone, m.p.=59°-61° C.
後処理
- temperaturewas heated
- temperatureat reflux for 6 hours
- customAt the end of the reaction
- customthe solvent was removed on a rotary evaporator
- extractionthe crude solid was extracted into dichloromethane (750 ml)
- filtrationThe insoluble inorganics were filtered off
- concentrationThe dichloromethane solution was concentrated again to a crude oil (34.5 g)
- customPurification
- washwas effected by flash chromatography over a silica gel column (SiO2, 150 g; eluted with 7:3 hexane:dichloromethane, 2 l; and dichloromethane 2 l)
- customThe material thus purified
- customwas recrystallized from ethanol
- customRecrystallization again from ethanol
出典と根拠
- ORDレコード
- ord-e9f21ffe3846464cba8dbc6267eeeb06
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05591745
関連ノート
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