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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276006Generated: October 30, 2026

Oxalyl chloride → HCID 18680910, compound

https://huagongshe.com/reaction/276006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18681159HCID 18681159—
CatalystDichloromethaneHCID 6344—
SolventDimethylformamideHCID 6228—
ProductHCID 18680910HCID 18680910—

Reaction Steps

Oxalyl chloride (0.208 ml) was added dropwise to a suspension prepared by adding 390 mg of 6-carboxy-1-(2-chlorobenzyl)-2-cyclopropylbenzimidazole to 10 ml of methylene chloride containing 1 drop of N,N-dimethylformamide at room temperature over a period of several minutes. The mixture was stirred at the same temperature for 2 hours, and was then concentrated under reduced pressure. Isopropyl ether was added to the residue, and the mixture was pulverized to give 450 mg of 1-(2-chlorobenzyl)-6-chlorocarbonyl-2-cyclopropylbenzimidazole hydrochloride (60) as a white powder. Since this product was unstable, it was used as a starting material in the subsequent step without being purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-a2ba4306d8044ec5b620c73916a02a7d
Source noteuspto-grants-2002_03