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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980908Generated: October 30, 2026

Diisopropylamine → 2-Acetyl-4-(4-pyridyl)cyclohexanone

https://huagongshe.com/reaction/980908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2-AcetylimidazoleHCID 538972—
ReactantCyclohexanone, 4-(4-pyridinyl)-HCID 10154273—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Acetyl-4-(4-pyridyl)cyclohexanoneHCID 1377205566.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3.2 ml of diisopropylamine dissolved in 40 ml of tetrahydrofuran, there was added 14.2 ml of 1.6M solution of n-butyl lithium in hexane at -20° C. Then, a solution of 2 g of 4-(4-pyridyl)cyclohexanone dissolved in 40 ml of tetrahydrofuran was added at -40° C. The reaction mixture was cooled to -78° C., and 2.5 g of acetylimidazole dissolved in 40 ml of tetrahydrofuran was added. The reaction mixture was stirred at room temperature, poured into ice water, and then washed with ether. The aqueous layer was saturated with ammonium chloride and extracted with methylene chloride. Thus, there was obtained 1.65 g of 2-acetyl-4-(4-pyridyl)cyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639521
Source datasetuspto-grants-1987_01
ORD IDord-0db94c5d2858435699da62e6e0524781
Source noteuspto-grants-1987_01