تفاعل #1596947
ord-3d5c2e053fc14ce78b8460cad8562c14
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىthe organic phase is separated off
- 2استخلاصThe aqueous phase is extracted with toluene
- 3غسيلthe combined organic phases are washed successively with water, saturated sodium hydrogen-carbonate solution and saturated sodium chloride solution
- 4أخرىThe solution is dried
- 5تركيزconcentrated to dryness
- 6أخرىThe crude product is purified by column chromatography (SiO2, n-heptane:toluene=2:1)
الإجراء التجريبي
72.9 g (0.16 mol) of bismuth(III) bromide are initially introduced in 50 ml of toluene at −10° C., and a solution of 50.0 g (0.25 mol) of 4-bromo-3-fluorobenzaldehyde in 250 ml of toluene is added dropwise. A solution of 27.0 g (0.27 mol) of 2-ethylbut-3-en-1-ol in 50 ml of toluene is metered in at this temperature, and the mixture is stirred at 10° C. for 2 h. Dilute hydrochloric acid is added to the batch, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed successively with water, saturated sodium hydrogen-carbonate solution and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:toluene=2:1), giving 4-bromo-2-(4-bromo-3-fluorophenyl)-5-ethyltetrahydropyran as a colourless oil.