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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274075Generated: October 31, 2026

Trityl chloride → [1-(triphenylmethyl)-1H-imidazol-4-yl]methanol

https://huagongshe.com/reaction/1274075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178519868HCID 178519868—
SolventAcetonitrileHCID 6342—
Product[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 38218282.3%

Reaction Steps

Diisopropylethylamine (14 mL, 80 mmol) was added dropwise to a suspension of 4-imidazole methanol (5.4 g, 40 mmol) in CH3CN (15 mL) at 0° C. A homogeneous yellow solution was formed. To this solution was added triphenylmethyl chloride (11.2 g, 40 mmol). The reaction mixture was stirred at room temperature for 2 h. The resultant white precipitate was filtered and washed successively with saturated NaHCO3 aqueous solution (2×20 mL) and water (2×20 mL), then dried in a vacuum oven (45° C.) for 12 h to afford a white solid 11.2 g (82%) which was used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156746
Source datasetuspto-grants-2000_12
ORD IDord-397216c9a0894548895890bc7da0dfe8
Source noteuspto-grants-2000_12