تفاعل #1596947

ord-3d5c2e053fc14ce78b8460cad8562c14

معادلة التفاعل

Cl
hydrochloric acid
[Br][Bi]([Br])[Br]
bismuth(III) bromide
O=Cc1ccc(Br)c(F)c1
4-bromo-3-fluorobenzaldehyde
C=CC(CC)CO
2-ethylbut-3-en-1-ol
CCC1COC(c2ccc(Br)c(F)c2)CC1Br
4-bromo-2-(4-bromo-3-fluorophenyl)-5-ethyltetrahydropyran

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe organic phase is separated off
  2. 2
    استخلاصThe aqueous phase is extracted with toluene
  3. 3
    غسيلthe combined organic phases are washed successively with water, saturated sodium hydrogen-carbonate solution and saturated sodium chloride solution
  4. 4
    أخرىThe solution is dried
  5. 5
    تركيزconcentrated to dryness
  6. 6
    أخرىThe 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08211513B2uspto-grants-2012_07