Water → 1-Bromo-6-methoxyhexane
反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]Br.[CH3:9][O-:10].[Na+].CCCCCC.O>CO>[CH3:9][O:10][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][Br:1]参加物
実験手順
6-Bromohexyl methyl ether was prepared from 1,6-dibromohexane. To 48.8 g (200 mmol) of 1,6-dibromohexane at 60° C. was added 44 g (200 mmol) of a 25% solution of sodium methoxide in methanol. The reaction mixture was held 0.5 hours, then an additional 4 g of sodium methoxide solution was added, and the reaction mixture was held an additional hour. Hexane and water were added, the organic phase was washed with brine and dried with magnesium sulfate, filtered and stripped. Fractional distillation under vacuum gave 93% pure 6-bromohexyl methyl ether. This bromide was converted to the Grignard reagent, which was converted to 1-(7-methoxyheptyl)-cyclopropene in the same manner that pentylmagnesium bromide was converted to 1-hexylcyclopropene.
後処理
- waitthe reaction mixture was held an additional hour
- washthe organic phase was washed with brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- distillationFractional distillation under vacuum
出典と根拠
- ORDレコード
- ord-01faa00a5ee743848313ef65f3dfd14c
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06365549B2
反応ノート
読み込み中…