Reacción #2146733
ord-bbafd291e0814f8194d482de053075ac
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONAfter complete addition
- 2workup.STIRRINGStirring
- 3workup.WAITwas continued a further 15 min at −10° C., before the cooling bath
- 4Otrowas removed
- 5workup.STIRRINGAfter 3 h of stirring at room temp.
- 6workup.ADDITIONthe reaction mixture was poured into 1 L of water
- 7Otrothe organic layer separated
- 8Extracciónaqueous one extracted twice with 1 L of ether each
- 9LavadoThe combined organic extracts were washed with water and brine
- 10Secadodried with sodium sulphate
- 11Concentraciónconcentrated under reduced pressure
- 12OtroThe crude material (191 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 19:1, Rf=0.40)
Procedimiento
Under an atmosphere of nitrogen, a solution of 46.3 g (413 mmol) of potassium tert-butoxide in 250 mL of dry THF was a added between −15° C. and −10° C. to a stirred mixture of 150 g (376 mmol) butyl triphenylphosphonium bromide in 500 mL of dry THF. After complete addition, stirring was continued at −10° C. for 30 min, prior to the dropwise addition of 65.3 g (413 mmol) of 3-methyl-5-oxopentyl acetate in 250 mL of dry THF within a period of 30 min. Stirring was continued a further 15 min at −10° C., before the cooling bath was removed and the reaction mixture was allowed to warm to room temp. After 3 h of stirring at room temp., the reaction mixture was poured into 1 L of water, the organic layer separated and aqueous one extracted twice with 1 L of ether each. The combined organic extracts were washed with water and brine, dried with sodium sulphate, and concentrated under reduced pressure. The crude material (191 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 19:1, Rf=0.40) to afford 57.9 g (78%) of (5Z)-3-methylnon-5-enyl acetate as a colourless liquid.