Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653969Generated: October 25, 2026

4-Tert-butylcyclohexane-1-carboxylic acid → 4-tert-Butylcyclohexylmethanol

https://huagongshe.com/reaction/653969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Tert-butylcyclohexane-1-carboxylic acidHCID 136759—
SolventTetrahydrofuranHCID 8028—
Product4-tert-ButylcyclohexylmethanolHCID 8275999%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-tert-butylcyclohexane carboxylic acid (10.0 g, 54.3 mmol of a mixture of cis and trans isomers) in anhydrous THF (distilled over Na/benzophenone) (44 mL) at 0° C., under argon were added dropwise B2H6 in THF (66.5 mL of 0.98M, 65.2 mmol). The reaction mixture was stirred at 0° C. for 2 hrs and then placed in the freezer overnight. The reaction was quenched by addition of saturated NaCl solution (50 mL) and was concentrated. The aqueous residue was extracted with EtOAc (3×200 mL) and the combined organic extracts were washed with sat. NaHCO3 solution (250 mL), followed by saturated brine (250 mL), dried over Na2SO4, and filtered. Concentration to dryness yielded 9.96 g of crude product which was purified via flash chromatography eluting with 25% EtOAc in hexane to yield an amorphous 4-(1,1-dimethylethyl)cyclohexanemethanol (9.18 g, 53.9 mmol) as a mixture of cis and trans isomers in 99% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128448
Source datasetuspto-grants-1992_07
ORD IDord-1456051eead44124bf6a1130c7f4f683
Source noteuspto-grants-1992_07