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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462208Generated: October 25, 2026

Trityl chloride → 1-[1-(2-Trityloxyphenyl)vinyl]imidazole

https://huagongshe.com/reaction/1462208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant2-[1-(1H-imidazol-1-yl)vinyl]phenolHCID 2805536—
SolventDichloromethaneHCID 6344—
Product1-[1-(2-Trityloxyphenyl)vinyl]imidazoleHCID 1334495745.6%

Reaction Steps

To a suspension of 1-[1-(2-hydroxyphenyl)vinyl]imidazole (500 mg) and triethylamine (407 mg) in dry methylene chloride (5 ml) is added trityl chloride (1.12 g) under stirring at room temperature, and the mixture is stirred at room temperature for 1 hour. To the mixture ice water is added and extracted with methylene chloride. The methylene chloride extract is dried on anhydrous sodium sulfate, and then concentrated. The residue is chromatographed on a column of silica gel, and eluted with methylene chloride-methanol (3-5%). The eluate is concentrated and the residue is crystallized from isopropyl ether and a small amount of petroleum ether to give 1-[1-(2-trityloxyphenyl)vinyl]imidazole (525 mg). mp. 149°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459412
Source datasetuspto-grants-1984_07
ORD IDord-c7422d7c15cc43c9a58ce23972d6fdb3
Source noteuspto-grants-1984_07