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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236844Generated: October 30, 2026

Ethanol → Diethyl methyl(3-oxocyclohexyl)malonate

https://huagongshe.com/reaction/236844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Cyclohexen-1-oneHCID 13594—
ReactantHCID 5088009HCID 5088009—
ReactantSodiumHCID 5360545—
SolventAcetic AcidHCID 176—
ProductDiethyl methyl(3-oxocyclohexyl)malonateHCID 103616—

Reaction Steps

Into a 2 l. 3-neck flask equipped with stirrer, condenser, thermometer, dropping funnel, and under a nitrogen atmosphere is placed 325 ml. of ethanol, and 2.5 g. of freshly cut sodium is added. When solution of the sodium is effected, 200 g. of diethyl methyl malonate is added in 5 minutes, and the mixture is stirred at room temperature for 1 hour. At the end of this period a solution of 100 g. of 2-cyclohexen-1-one in 130 ml. of ethanol is added through the dropping funnel over a period of 1 hour. The ensuing mild exothermic reaction causes the temperature to rise to 42° C. Stirring is continued overnight at room temperature, after which 20 ml. of acetic acid is added, and the mixture is evaporated at reduced pressure. The residual oil is dissolved in 1.31 l. of ether, transferred to a separatory funnel and washed with three 230 ml. portions of water. The ether solution is dried over anhydrous sodium sulfate, filtered, and dried over anhydrous calcium sulfate. The ether is removed at reduced pressure and the residual oil distilled under high vacuum using a 6-inch Vigreux column. After removal of a forerun of 22.5 g., bp 49°-129°/0.14-0.21 mm, α-methyl-3-oxocyclohexane malonic acid diethyl ester distills at 129°-130°/0.2 mm; 211.5 g, 75.4% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04158007
Source datasetuspto-grants-1979_06
ORD IDord-cef26bfb13e64e14baff202f0b749538
Source noteuspto-grants-1979_06