Reacción #1772045

ord-381964c8b7fd4185ac23769bb2c99b53

Ecuación de reacción

[Mg]
Magnesium
FC(F)(F)CCCBr
4-bromo-1,1,1-trifluorobutane
O=Cc1ccc(Br)cc1
4-bromobenzaldehyde
OC(CCCC(F)(F)F)c1ccc(Br)cc1
1-(4-bromophenyl)-5,5,5-trifluoropentan-1-ol
Rendimiento 82.2%

Disolventes

Condiciones de reacción

Temperatura
24°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe cold bath was removed
  2. 2
    Temperaturato warm
  3. 3
    workup.STIRRINGstirred 18 h
  4. 4
    workup.ADDITIONdiluted with Et2O (1 vol)
  5. 5
    Otroquenched with sat'd NH4Cl soln
  6. 6
    Lavadowashed with brine
  7. 7
    ConcentraciónConcentrate
  8. 8
    workup.ADDITIONcharged to a 40M Biotage® silica gel cartridge
  9. 9
    LavadoGradient elution

Procedimiento

Magnesium (0.636 g, 26.2 mmol) was added to a solution of 4-bromo-1,1,1-trifluorobutane (5 g, 26.2 mmol) in THF (100 mL) and under nitrogen. The solution was stirred for 18 h at 24° C., and the Grignard reagent was transferred via cannula to a solution of 4-bromobenzaldehyde (4.85 g, 26.2 mmol) in THF (50 mL) at −78° C. under nitrogen. The cold bath was removed and the reaction allowed to warm and stirred 18 h, diluted with Et2O (1 vol), quenched with sat'd NH4Cl soln, and washed with brine. Concentrate, take up in CH2Cl2 and charged to a 40M Biotage® silica gel cartridge. Gradient elution was performed from 15% to 100% B over 1 L (A/B Hexanes/EtOAc) to give 1-(4-bromophenyl)-5,5,5-trifluoropentan-1-ol 6.4 g (82%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08147818B2uspto-grants-2012_04