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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178106Generated: October 27, 2026

Water → 4-Iodo-1-(triphenylmethyl)-1H-pyrazole

https://huagongshe.com/reaction/1178106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant4-IodopyrazoleHCID 77022—
SolventDichloromethaneHCID 6344—
Product4-Iodo-1-(triphenylmethyl)-1H-pyrazoleHCID 1532447926.4%

Reaction Steps

Trityl chloride (885 mg, 3.2 mmol) was added to a stirred cold (0-5° C.) solution of 4-iodo pyrazole (513 mg, 2.6 mmol) and triethylamine (401 mg, 0.55 mL, 0.4 mmol) in DCM (10 mL). Stirring was continued at room temperature overnight. Cold water was then added and the product was extracted with DCM and the organic layer was washed with sat. sodium bicarbonate solution followed by brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure to get the residue. The obtained residue was purified by column chromatography (using neutral alumina and 2% EtOAc in Hexane as eluent) to afford 300 mg (26% yield) of 4-iodo-1-trityl-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-c0911932a8a14541b03846a42bfa6631
Source noteuspto-grants-2010_11