Reacción #833543
ord-512f3ad52a0a49789b2cd56cfe540af4
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroReaction mixture
- 2Otroadditional 1 hr
- 3Otroat RT
- 4workup.ADDITIONAfter that time the resulted mixture was poured
- 5workup.STIRRINGwith stirring, into a vessel
- 6ExtracciónOrganic compounds were extracted with 3×200 ml of ether
- 7Secadodried over sodium sulfate
- 8OtroAfter removal of ether material
- 9workup.DISSOLUTIONwas dissolved in minimum amount of dichloromethane
- 10Otropurified by silica gel chromatography (100% dichloromethane as eluent)
Procedimiento
Under inert atmosphere 10 ml of BH3 THF complex (1.0 M THF solution) were added to 30 ml THF solution of 2.15 gr (6.41 mmole) of 16-bromohexadecanoic acid at −20° C. Reaction mixture was stirred at this temperature for 2 hrs and then additional 1 hr at RT. After that time the resulted mixture was poured, with stirring, into a vessel containing 200 ml of ice/saturated sodium bicarbonate aqueous solution. Organic compounds were extracted with 3×200 ml of ether. The ether fractions were combined and dried over sodium sulfate. After removal of ether material was dissolved in minimum amount of dichloromethane and purified by silica gel chromatography (100% dichloromethane as eluent). 1.92 gr (93% yield) of the desired product were obtained.