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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365041Generated: October 30, 2026

2,4-Dimethoxybenzaldehyde → HCID 66971332, compound

https://huagongshe.com/reaction/1365041

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 numberUS07888487B2
Source datasetuspto-grants-2011_02
ORD IDord-2d5b797a4f1f4e2b89eba4b84a526e82
Source noteuspto-grants-2011_02