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HRID 653969作成日:2026年10月26日

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

https://huagongshe.com/reaction/653969

反応式

関与物質

役割名称HCID仕込み量
反応物4-Tert-butylcyclohexane-1-carboxylic acidHCID 136759—
溶媒TetrahydrofuranHCID 8028—
生成物4-tert-ButylcyclohexylmethanolHCID 8275999%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05128448
出典データセットuspto-grants-1992_07
ORD IDord-1456051eead44124bf6a1130c7f4f683
出典メモuspto-grants-1992_07