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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992682Generated: November 2, 2026

Trityl chloride → Ethyl 1-tritylpyrazole-4-carboxylate

https://huagongshe.com/reaction/992682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
ReactantWater ethylacetateHCID 22728543—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-tritylpyrazole-4-carboxylateHCID 1052396879.5%

Reaction Steps

Under N2 atmosphere, potassium tert-butoxide (9.60 g, 85.5 m mol) and trityl chloride (21.9 g, 78.5 m mol) were added successively to a solution of 4-(ethoxycarbonyl)pyrazole (10.0 g, 71.3 m mol) in DMF (100 ml) at 0° C. After stirred for 1 hour, the mixture was poured into water/ethyl acetate. The aqueous layer was separated, and the organic layer was washed with water, brine and dried over magnesium sulfate. After evaporation of the solvent, the resulting precipitate was recrystallized from ethyl acetate to afford 4-ethoxycarbonyl-1-(trityl)pyrazole (21.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468995B1
Source datasetuspto-grants-2002_10
ORD IDord-4f0cfd2035d048d49bcc4289b5b6845b
Source noteuspto-grants-2002_10