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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636813Generated: October 29, 2026

Trityl chloride → Ethyl 1-trityl-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/1636813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 178469898HCID 178469898—
SolventChloroformHCID 6212—
ProductEthyl 1-trityl-1H-imidazole-4-carboxylateHCID 618225—

Reaction Steps

A suspension of ethyl imidazole-4-carboxylate (1.4 g), triethylamine (1.2 g) and chloroform (20 ml) was stirred at room temperature while trityl chloride (3.06 g) was added, and the mixture was stirred at room temperature for 1 h. The resulting solution was washed with water, dried and evaporated to dryness under reduced pressure, and the residue was crystallised from a mixture of ethyl acetate and cyclohexane, to give ethyl 1-tritylimidazole-4-carboxylate, mp 163°-164°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036617
Source datasetuspto-grants-2000_03
ORD IDord-91ce51a165e840c2a0015a804d1ff624
Source noteuspto-grants-2000_03