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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614922Generated: October 30, 2026

Hydrochloric Acid → (1S)-4-methylcyclohex-3-ene-1-carboxylic acid

https://huagongshe.com/reaction/1614922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(1S)-4-methylcyclohex-3-ene-1-carboxylic acidHCID 1087719091%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-Methyl-cyclohex-3-(S)-enecarboxylic acid 4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester (3.34 g, 13.2 mmol) in THF (25 mL), water (2.5 mL) and methanol (2.5 mL) was treated with lithium hydroxide monohydrate (2.8 g, 66.2 mmol) and warmed to 50° C. with stirring. After 1 h, the reaction mixture treated with 1M HCl (about 25 mL). The mixture was extracted with hexanes:ethyl acetate (200 mL: 15 mL), dried over sodium sulfate, filtered and concentrated to 2.4 g of a white semi-solid. The residue was redissolved in hexanes:dichloromethane (100 mL, 95:5), washed with water, dried over sodium sulfate, filtered and concentrated to 1.68 g (91% yield) of (1S)-4-methyl-cyclohex-3-enecarboxylic acid as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765722B2
Source datasetuspto-grants-2014_07
ORD IDord-4692d8173d0847638ed8f5148ec32cb5
Source noteuspto-grants-2014_07