Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350868Generated: October 25, 2026

Benzoyl chloride → HCID 178490912, compound

https://huagongshe.com/reaction/350868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCalcium HydroxideHCID 6093208—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 178490910HCID 178490910—
CatalystWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178490912HCID 178490912—

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution containing 1.0 g of 2-(4-methoxybenzyl)-5-methyl-2H-pyrazol-3-ol in 30 ml of dioxan was treated with 679 mg of calcium hydroxide and 800μl of benzoyl chloride, then heated at 110° C. for 2 h. To the mixture was added 20 drops of water and the mixture heated for a further 2 h. The solvent was evaporated under reduced pressure and the residue partitioned between dichloromethane/10% citric acid. The organic phase was washed with brine, then dried over anhydrous magnesium sulphate, filtered and evaporated to give yellow oil. The oil was purified twice by flash chromatography on silica gel, initially using methanol/dichloromethane (1:49) to give a red solid, then ethyl acetate/ hexane (1:1 to 2:1) for the elutions to give 400 mg of [5-hydroxy-1-(4-methoxybenzyl)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone as a yellow gum. Mass spectrum (ES) m/z 323 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183296B2
Source datasetuspto-grants-2007_02
ORD IDord-4bf8308175894dd1a2c7ad659d70a972
Source noteuspto-grants-2007_02