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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223837Generated: October 26, 2026

Hydrochloric Acid → Methyl 1-allylcyclohexanecarboxylate

https://huagongshe.com/reaction/2223837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl bromideHCID 7841—
ReactantMethyl cyclohexanecarboxylateHCID 20748—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-allylcyclohexanecarboxylateHCID 1093206718.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of methyl cyclohexylcarboxylate (1.42 g) and allyl bromide (3.02 g) in N,N-dimethylformamide (20 mL) was added potassium tert-butoxide (1.68 g, 15.0 mmol) under ice cooling. The solution was stirred at room temperature for 16 hours, at 50° C. for 8 hours and further at room temperature for 64 hours. Water and 3N hydrochloric acid were then added to the solution, and it was extracted with diethyl ether. The extract was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by column chromatography (silica gel, hexane:ethyl acetate=97:3) to give the title compound (340 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375115B2
Source datasetuspto-grants-2008_05
ORD IDord-babd89385a2046c38f7579c3b285f050
Source noteuspto-grants-2008_05