Reacción #336305

ord-8055d168db824518b0599ab852eb2409

Ecuación de reacción

CC(C)=CCC/C(C)=C/CC/C(C)=C/CO
(E,E)-farnesol
CC(C)=CCCC(C)=CCCC(C)=CCN1C(=O)c2ccccc2C1=O
1
CC(C)=CCCC(C)=CCCC(C)=CCN1C(=O)c2ccccc2C1=O
2-(3,7,11-Trimethyl-2,6,10-dodecatrienyl)-1H-isoindole-1,3(2H)-dione
BrP(Br)Br
PBr3
CC(C)=CCCC(C)=CCCC(C)=CCBr
farnesyl bromide

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroquenched with H2O
  2. 2
    Otroseparated
  3. 3
    LavadoThe organic phase was washed with 15 ml of NaHC03, 15 ml of H2O, and 15 ml of brine
  4. 4
    Secadodried over MgSO4
  5. 5
    Otroevaporated

Procedimiento

A solution of 2.00 g (9.0 mmol) of (E,E)-farnesol in 20 ml of dry diethyl ether at 0° C. under argon in the dark was treated dropwise with a solution of 735 1 (4.0 mmol, 0.45 eq.) of PBr3 in 4 ml of dry diethyl ether. The resultant mixture was stirred at 0° C. for one hour, then quenched with H2O and separated. The organic phase was washed with 15 ml of NaHC03, 15 ml of H2O, and 15 ml of brine, dried over MgSO4 and evaporated to provide 2.47 g of crude farnesyl bromide as a clear oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05212164uspto-grants-1993_05