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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475127Generated: October 30, 2026

3,4-dihydro-2H-pyran → 4-bromo-6-chloro-2-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/475127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant4-Bromo-6-chloro-2-methyl-1H-benzo[d]imidazoleHCID 53216860—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-6-chloro-2-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazoleHCID 7127250869.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 4-bromo-6-chloro-2-methyl-1H-benzo[d]imidazole (3.5 g, 14.26 mmol), p-TsOH.H2O (272 mg, 1.43 mmol), and 3,4-dihydro-2H-pyran (5.9 g, 71.30 mmol) in THF (20 mL) was stirred at 75° C. for 4 h. The reaction mixture was concentrated in vacuo and water was added. The mixture was extracted with EtOAc and the combined extracts dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by SiO2 chromatography eluting with a DCM:MeOH gradient (0 to 9% MeOH) to afford 4-bromo-6-chloro-2-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazole as a white solid (3.2 g, 69.6%). MS (ESI): m/z=329.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637537B2
Source datasetuspto-grants-2014_01
ORD IDord-b174f21846b84758a673258c3b84e2d5
Source noteuspto-grants-2014_01