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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405457Generated: November 3, 2026

Dichloromethane → HCID 67607839, compound

https://huagongshe.com/reaction/2405457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl AcetateHCID 8857—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 67891722HCID 67891722—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
ProductHCID 67607839HCID 67607839—

Reaction Steps

2.1 g (5.7 mmol) of N-[2-(3-bromophenylamino)phenyl]benzamide was suspended in 30 mL of xylene. After the addition of 0.6 g (2.9 mmol) of p-toluenesulfonic acid monohydrate, the mixture was subjected to azeotropic dehydration under heat reflux for 3 hours. After allowing the reaction solution to cool, ethyl acetate, methylene chloride, and water were added to the reaction solution, and an insoluble component was removed by filtration. The organic phase was extracted from the mother filtrate, washed with water and a saturated sodium chloride solution, and dried over magnesium sulfate. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1-(3-bromophenyl)-2-phenyl-1H-benzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08803420B2
Source datasetuspto-grants-2014_08
ORD IDord-ad7c013df0264650925c5a1de58d5b9d
Source noteuspto-grants-2014_08