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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665228Generated: October 26, 2026

p-Toluenesulfonic acid monohydrate → 7-[1-Ethylprop-1-en-1-yl]-2-(mesitylmethyl)-1-methyl-1H-benzimidazole

https://huagongshe.com/reaction/1665228

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-[2-(Mesitylmethyl)-1-methyl-1H-benzimidazol-7-yl]pentan-3-olHCID 24986430—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
Product7-[1-Ethylprop-1-en-1-yl]-2-(mesitylmethyl)-1-methyl-1H-benzimidazoleHCID 67438940—

Reaction Steps

A solution of 3-[2-(mesitylmethyl)-1-methyl-1H-benzimidazol-7-yl]pentan-3-ol (200 mg, 0.571 mmol) and p-toluenesulfonic acid monohydrate (326 mg, 1.71 mmol) in xylene (10 mL) was refluxed for 3 hr. After cooling, the mixture was diluted with ethyl acetate (50 mL) and washed with saturated aqueous sodium bicarbonate solution (30 mL) and brine (30 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with 10-20% ethyl acetate/n-hexane gradient mixture to give the title compound (180 mg, 0.542 mmol, 95%, as a mixture of geometric isomers) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039500B2
Source datasetuspto-grants-2011_10
ORD IDord-4156e820019b42d6a64b96a7c41f8f71
Source noteuspto-grants-2011_10