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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993145Generated: November 2, 2026

Hexane → Methyl 4-formylcyclohexane-1-carboxylate

https://huagongshe.com/reaction/1993145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 59133005HCID 59133005—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-formylcyclohexane-1-carboxylateHCID 1125225397.1%

Reaction Steps

103 g of methyl 4-methoxymethylidene-cyclohexane-carboxylate was dissolved in 350 mL of THF, to which 100 mL of 10% hydrochloric acid was added dropwise at 11 to 13° C. for 10 minutes. The solution was further stirred at room temperature for 3 hours, and then 80 mL of hexane was added. The water phase was extracted with ethyl acetate, and then the organic phases were combined and washed with water and saturated saline in this order. The resultant product was dried over anhydrous magnesium sulfate, and then concentrated, to obtain 92.4 g of methyl 4-formylcyclohexane-carboxylate in the form of an oil-like product. The obtained product was analyzed by gas chromatography, and was found to be a mixture of cis-form: trans-form at a ratio of 64:36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07651630B2
Source datasetuspto-grants-2010_01
ORD IDord-10ffe03360fa4b61a150027350c2e5ab
Source noteuspto-grants-2010_01