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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349520Generated: October 30, 2026

Trityl chloride → 1-Methyl-5-triphenylmethylaminopyrazole-4-carbaldehyde

https://huagongshe.com/reaction/349520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant5-amino-1-methyl-1H-pyrazole-4-carbaldehydeHCID 12332515—
SolventDichloromethaneHCID 6344—
Product1-Methyl-5-triphenylmethylaminopyrazole-4-carbaldehydeHCID 1796196092%

Reaction Steps

To a suspension of 5-amino-1-methylpyrazole-4-carbaldehyde (25 g, 200 mmol) and triethylamine (22.2 g, 220 mmol) in dichloromethane (500 ml) was added triphenylmethyl chloride (61.3 g, 220 mmol) at room temperature. The mixture was stirred at room temperature for 70 hours. The reaction mixture was washed with successively 10% aqueous citric acid solution, brine and 10% aqueous sodium hydrogencarbonate solution. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with ethyl acetate to give 1-methyl-5-triphenylmethylaminopyrazole-4-carbaldehyde (67.6 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-7f51fab0e18d4d4884f734fa07597ce2
Source noteuspto-grants-2007_02