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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699603Generated: November 1, 2026

Oxalyl chloride → HCID 18680910, compound

https://huagongshe.com/reaction/1699603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18681159HCID 18681159—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18680910HCID 18680910—

Reaction Steps

A suspension is prepared by adding 6-carboxy-1-(2-chlorobenzyl)-2-cyclopropylbenzimidazole (390 mg) to methylene chloride (10 ml) which includes N,N-dimethylformamide (one drop). Oxalyl chloride (0.208 ml) is dripped into the suspension over a period of a few minutes at room temperature. After stirring for two hours at the same temperature, the mixed material is concentrated under reduced pressure. Isopropyl ether is added to the residue, which is then turned into powder. Thus, white powder of 1-(2-chlorobenzyl)-6-chlorocarbonyl-2-cyclopropylbenzimidazole hydrochloride (450 mg) is obtained. Because this material is unstable, it is used as a source material for the next process without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348032B1
Source datasetuspto-grants-2002_02
ORD IDord-6ff52d03c5a84ffa97d0b89827737dcf
Source noteuspto-grants-2002_02