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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131633Generated: October 25, 2026

Chlorodiphenylmethane → 1-(Diphenylmethyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/131633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodiphenylmethaneHCID 7035—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(Diphenylmethyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 69313438—

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 1H-pyrazole-4-carboxylic acid ethyl ester (1.0 g), benzhydryl chloride (1.9 ml) and potassium carbonate (1.48 g) in anhydrous 1-methyl-2-pyrrolidinone (10 ml) was heated at 100° C. under nitrogen for 6 h. It was diluted with water and extracted with ethyl acetate, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (4:1) followed by i-hexane/ethyl acetate (2:1) to give the sub-title compound (2.18 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384951B2
Source datasetuspto-grants-2008_06
ORD IDord-b9eb24beb22d458e8dd7dc49124f29a9
Source noteuspto-grants-2008_06