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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285408Generated: October 31, 2026

Diethyl Malonate → Diethyl (cyclohex-2-en-1-yl)propanedioate

https://huagongshe.com/reaction/1285408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactanttrans-1,2-DibromocyclohexaneHCID 98506—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductDiethyl (cyclohex-2-en-1-yl)propanedioateHCID 237534—

Reaction Steps

Within 2 hours, 1.1 l of ethanol was added dropwise to 69 g of finely chopped sodium in a 2-liter three-necked flask equipped with dropping funnel, reflux condenser, and agitator. The hot alcoholate solution was combined dropwise--again within 2 hours--with 196 g of diethyl malonate. After allowing the reaction mixture to cool, 296 g of trans-1,2-dibromocyclohexane was added--within 2 hours--to the reaction solution, which latter was then boiled under reflux overnight. After concentration of the reaction solution on a forced circulation evaporator, the residue was combined with ether and dilute hydrochloric acid, the organic phase then washed with saturated sodium chloride solution, concentrated, and distilled under vacuum, thus obtaining 197 g, bp1 119°-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567195
Source datasetuspto-grants-1986_01
ORD IDord-4ffaeaa8626247d991efded4a1f9652e
Source noteuspto-grants-1986_01