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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 653969Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/653969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Tert-butylcyclohexane-1-carboxylic acidHCID 136759—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-tert-ButylcyclohexylmethanolHCID 8275999%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05128448
Quelldatensatzuspto-grants-1992_07
ORD IDord-1456051eead44124bf6a1130c7f4f683
Quellennotizuspto-grants-1992_07