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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102328Generated: October 31, 2026

2,4-Dimethoxybenzaldehyde → HCID 66971332, compound

https://huagongshe.com/reaction/2102328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantHCID 23079539HCID 23079539—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66971332HCID 66971332—

Reaction Steps

To a solution of 3-benzyloxy-4-bromo-1-isopropyl-5-(4-methoxyphenyl)-1H-pyrazole in tetrahydrofuran (2 mL) was added n-butyllithium (2.6 mol/L hexane solution, 0.89 mL) at −78° C. under argon atmosphere, and the mixture was stirred for 30 minutes. A solution of 2,4-dimethoxybenzaldehyde (0.51 g) in tetrahydrofuran (2 mL) was added to the reaction mixture, and the mixture was stirred at −78° C. for 1 hour. The reaction mixture was directly purified by column chromatography on aminopropylated silica gel (eluent:tetrahydrofuran). The obtained semi purified [3-benzyloxy-1-isopropyl-5-(4-methoxyphenyl)-1H-pyrazol-4-yl (2,4-dimethoxyphenyl)methanol was dissolved in ethanol (9 mL), and a catalytic amount of 10% palladium-carbon powder was added to the solution. The mixture was stirred at room temperature under a hydrogen atmosphere overnight. Dichloromethane was added to the reaction mixture, and the insoluble material was removed by filtration. The solvent of the filtrate was removed, and diethyl ether and hexane were added to the residue. The insoluble material was collected by filtration and dried under reduced pressure to give the title compound (0.09 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576063B2
Source datasetuspto-grants-2009_08
ORD IDord-0dfc5f80cf11439ca4505da7cc91d839
Source noteuspto-grants-2009_08