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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376304Generated: October 26, 2026

Acetone → 3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenal

https://huagongshe.com/reaction/1376304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
Reactant4-(4-Propylcyclohexyl)cyclohexaneHCID 17884097—
SolventHydrochloric AcidHCID 313—
Product3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenalHCID 12020437—

Reaction Steps

The resulting cyclohexane derivative was dissolved in a mixed solvent of acetone (80 ml) with 2N hydrochloric acid (8 ml), followed by heating the solution under reflux for 4 hours, cooling the reaction mixture down to room temperature after completion of the stirring, adding water, extracting with ether (50 ml), drying the organic layer over anhydrous magnesium sulfate, and concentrating under reduced pressure to obtain 3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenal (3.1 g, 12 mmols). This product was used in the subsequent reaction without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05662830
Source datasetuspto-grants-1997_09
ORD IDord-6b453bb4e3e94247abf5a6420bc92694
Source noteuspto-grants-1997_09