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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090937Generated: October 30, 2026

1046784-68-2 → cyclohexyl[1-(2-chlorophenyl)-3-methyl-1H-pyrazol-4-yl]methanol

https://huagongshe.com/reaction/2090937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1046784-68-2HCID 43381506—
ReactantHCID 178419651HCID 178419651—
SolventTetrahydrofuranHCID 8028—
Productcyclohexyl[1-(2-chlorophenyl)-3-methyl-1H-pyrazol-4-yl]methanolHCID 6677695379%

Reaction Steps

To a solution (5 mL) of 1-(2-chlorophenyl)-3-methyl-1H-pyrazole-4-carbaldehyde (0.27 g) synthesized in the above-mentioned (2) in tetrahydrofuran was added dropwise under ice-cooling cyclohexylmagnesium bromide (2.0 mL, 1M tetrahydrofuran solution). After the completion of the dropwise addition, the ice bath was removed, and the mixture was stirred at room temperature for 15 min. To the reaction mixture was added aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2, volume ratio) to give the title object compound (0.29 g, 79%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-ed8a2177630a421997aac9cdeda2e5c1
Source noteuspto-grants-2013_05