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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216351Generated: October 30, 2026

Trityl chloride → 4-(2,2-dimethylbut-3-en-1-yl)-1-trityl-1H-imidazole

https://huagongshe.com/reaction/216351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178442465HCID 178442465—
SolventDichloromethaneHCID 6344—
Product4-(2,2-dimethylbut-3-en-1-yl)-1-trityl-1H-imidazoleHCID 59140430—

Reaction Steps

Triethylamine (1.5 mL, 53 mmol) followed by of trityl chloride (9 g, 32 mmol) were added to a 0° C. solution of 4-(2,2-dimethylbut-3-en-1-yl)-1H-imidazole (4 g, 27 mmol) in methylene chloride (40 mL). After stirring at ambient temperature for 3 h, the reaction mixture was poured into saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were washed with brine, dried (magnesium sulfate), filtered and concentrated in vacuo. Chromatography over silica eluting with 10-40% ethyl acetate/hexane afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-c3bb28a95ff844f69ce54e4f1cca7f53
Source noteuspto-grants-2012_06