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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430325Generated: November 3, 2026

Cyclohexanone, 3,3-dimethyl- → 3,3-dimethyl-1-((5-methyl-1H-pyrazol-1-yl)methyl)cyclohexanol

https://huagongshe.com/reaction/1430325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanone, 3,3-dimethyl-HCID 76322—
Reactant1,5-DimethylpyrazoleHCID 136502—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3,3-dimethyl-1-((5-methyl-1H-pyrazol-1-yl)methyl)cyclohexanolHCID 86681330—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (−78° C.) solution of nBuLi (12.48 mL) in tetrahydrofuran (40 mL) was added a solution of 1,5-dimethyl-1H-pyrazole (3.0 g) in tetrahydrofuran (3 mL) dropwise. After stirring for 1 hour, a solution of 3,3-dimethylcyclohexanone (3.94 g) in tetrahydrofuran (3 mL) was added dropwise, and the reaction was allowed to warm to 0° C. After stirring for 1 hour, the reaction mixture was diluted with ether (100 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Purification of the residue by silica gel chromatography, eluting with a gradient of 3% to 25% ethyl acetate in hexanes, gave the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940737B2
Source datasetuspto-grants-2015_01
ORD IDord-290c5eba49e04f258aeff12d1ec61d41
Source noteuspto-grants-2015_01