تفاعل #2028899
ord-64f72b43543648c4939c1fdb8ec94732
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىwas kept at −40° C.
- 2workup.ADDITIONwere added dropwise
- 3درجة الحرارةAfter the reaction mixture had been slowly warmed up to room temperature
- 4أخرىit was quenched with a saturated aqueous solution of ammonium chloride
- 5workup.ADDITIONWater (1,000 ml) was then added
- 6أخرىto give two layers
- 7استخلاصThe water layer was extracted with toluene (500 ml) three times
- 8غسيلthe combined organic layer was washed with water
- 9تجفيفdried over anhydrous magnesium sulfate
- 10workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 11أخرىThe residue was purified by silica gel chromatography (silica gel: 300 g, eluent: toluene)
الإجراء التجريبي
THF (1,000 ml) was added to diisopropylamine (162.9 g) in a reaction vessel under an atmosphere of nitrogen. n-Butyllithium was added dropwise, while the solution was kept at −40° C. or lower, and the stirring was continued for 30 minutes. The solution was cooled at −65° C. or lower, and ethyl acetate (141.9 g) and then a THF (200 ml) solution of trans-4-propylcyclohexanecarboxylic acid chloride (2) (189.9 g) prepared in the first step were added dropwise. After the reaction mixture had been slowly warmed up to room temperature with stirring, it was quenched with a saturated aqueous solution of ammonium chloride. Water (1,000 ml) was then added to give two layers. The water layer was extracted with toluene (500 ml) three times, and the combined organic layer was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (silica gel: 300 g, eluent: toluene) to give 3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester (3) (220 g) in 90% yield.