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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881398Generated: November 1, 2026

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

https://huagongshe.com/reaction/1881398

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 numberUS08318767B2
Source datasetuspto-grants-2012_11
ORD IDord-97cc489fca5e4dd6bf7743457ecd4c55
Source noteuspto-grants-2012_11