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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352843Generated: October 25, 2026

Trityl chloride → methyl N-triphenylmethyl-5-benzimidazolecarboxylate

https://huagongshe.com/reaction/352843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactantmethyl 1H-benzimidazole-5-carboxylate hydrochlorideHCID 22710297—
SolventDichloromethaneHCID 6344—
Productmethyl N-triphenylmethyl-5-benzimidazolecarboxylateHCID 22710354106.7%

Reaction Steps

In dichloromethane (15 ml), methyl 5-benzimidazolecarboxylate hydrochloride (1.00 g) was suspended. To the resulting suspension, triethylamine (1.50 ml) and triphenylmethyl chloride (1.50 g) were added, followed by stirring at room temperature for 3 hours. The reaction mixture was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane:ethyl acetate=2:1), whereby title compound (2.10 g, quant.) was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-af0bf4a0bddb49e6b50c4a70c60ee1ea
Source noteuspto-grants-2004_06