반응 #2028899

반응 방정식

n-Butyllithium

trans-4-propylcyclohexanecarboxylic acid chloride

ethyl acetate

diisopropylamine

→

3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester

수율 91.0%

용매

THF

THF

반응 조건

후처리

1. 1
   기타was kept at −40° C.
2. 2
   workup.ADDITIONwere added dropwise
3. 3
   온도After the reaction mixture had been slowly warmed up to room temperature
4. 4
   기타it was quenched with a saturated aqueous solution of ammonium chloride
5. 5
   workup.ADDITIONWater (1,000 ml) was then added
6. 6
   기타to give two layers
7. 7
   추출The water layer was extracted with toluene (500 ml) three times
8. 8
   세척the combined organic layer was washed with water
9. 9
   건조dried over anhydrous magnesium sulfate
10. 10
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
11. 11
    기타The residue was purified by silica gel chromatography (silica gel: 300 g, eluent: toluene)

실험 절차

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.

출처