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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566238Generated: October 31, 2026

Trityl chloride → HCID 15475336, compound

https://huagongshe.com/reaction/566238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant2-(1H-Pyrazol-4-yl)ethanolHCID 4293604—
ReactantHCID 178520322HCID 178520322—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 15475336HCID 15475336—
Product2-[1-(Triphenylmethyl)-1H-pyrazol-4-yl]ethan-1-olHCID 15475337—

Reaction Steps

A mixture of 2-(3-pyrazolyl)ethanol and 2-(4-pyrazolyl)ethanol (2.4:1) (2.50 g) was dissolved in DMF (30 ml). To the solution were added, while stirring, triethylamine (2.26 g) and trityl chloride (6.22 g). The mixture was stirred at 25° C. for one hour, then at 40° C. for one hour. The reaction mixture was diluted with water, which was subjected to extraction with ethyl acetate. The organic layer was washed with an aqueous saline solution, which was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The concentrate was purified by means of a column chromatography (carrier: silica gel, 300 g, developing solvent: ethyl acetate-hexane, 1:1) to afford 2-(1-triphenylmethyl-3-pyrazolyl)ethanol (3.75 g) and 2-(1-triphenylmethyl-4-pyrazolyl)ethanol (1.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174877B1
Source datasetuspto-grants-2001_01
ORD IDord-5eb0e8ee898c4b9293039966ec2b7b64
Source noteuspto-grants-2001_01