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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621202Generated: October 31, 2026

Benzophenone → Benzimidazole

https://huagongshe.com/reaction/1621202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantDiisopropylethylamineHCID 81531—
ReactantAminoacetonitrile sulfate (1:1)HCID 196971—
SolventDichloromethaneHCID 6344—
ProductBenzimidazoleHCID 5798156,273.703%

Reaction Steps

To a stirred solution of 2-aminoacetonitrile bisulfate (2.9 g, 0.013 mmol) in dichloromethane (50 mL) was added benzophenone (3.48 mL, 0.0208 mmol) followed by DIEA (4.53 mL, 0.026 mmol). After stirring 18 h, the dichloromethane solution was washed with water (50 mL), dried over sodium sulfate, filtered, and the filtrate concentrated under reduced pressure. The residue was purified on a flash silica gel column (hexanes:EtOAc, 1:1) to give 3 (2.40 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772507B2
Source datasetuspto-grants-2014_07
ORD IDord-148ddf0856774f7bbd1db280c9c84c76
Source noteuspto-grants-2014_07