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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684812Generated: November 2, 2026

1-Methylcyclohexanecarboxylic acid → (1-Methylcyclohexyl)methanol

https://huagongshe.com/reaction/1684812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methylcyclohexanecarboxylic acidHCID 70744—
ReactantDiboronHCID 6328200—
SolventTetrahydrofuranHCID 8028—
Product(1-Methylcyclohexyl)methanolHCID 150184069%

Reaction Steps

To a solution of 1-methyl-1-hydroxycarbonylcyclohexane (10 g, 70 mmol) in tetrahydrofuran(300 mL) at 0° C. was added 1M diborane in tetrahydrofuran (200 mL, 200 mmol) over 90 minutes. The cooling bath was removed and the reaction mixture was stirred at room temperature for two days. The remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min with cooling. Additional saturated sodium bisulfate (200 mL) was added and after 20 min of stirring the aqueous layer was removed. The organic layer was washed with water and saturated sodium chloride, dried, filtered and concentrated. The residue was purified by flash chromatography using 20% diethylether in hexanes to give 1-methyl-1-hydroxymethylcyclohexane (6.17 g, 48 mmol, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043298E1
Source datasetuspto-grants-2012_04
ORD IDord-4e7dee2502b84ab18ecf35021b18dcc9
Source noteuspto-grants-2012_04