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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465048Generated: October 30, 2026

Thionyl Chloride → HCID 20261653, compound

https://huagongshe.com/reaction/465048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantHCID 13600722HCID 13600722—
ReactantHCID 20261709HCID 20261709—
SolventMethanolHCID 887—
ProductHCID 20261653HCID 20261653—

Reaction Steps

5-Chloromethyl-2-dimethylaminomethylbenzimidazole, 2hydrochloride (melting point 248.4° C., 3.64 g) was produced by subjecting 2-dimethylaminomethyl-5-hydroxymethylbenzimidazole (3 g) and thionylchloride (10.5 ml) to a 4-hour refluxing with heat. 2-Mercaptopropionitrile (1.05 g) was changed into sodium salt by sodium ethoxide and, at a temperature of 0° C., methanol solution of the above-mentioned chloromethyl compound was added gradually and the mixture was stirred through one whole night at the room temperature to yield 5-[(2-cyanoethyl)thiomethyl]-2-dimethylaminomethylbenzimidazole (3.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550118
Source datasetuspto-grants-1985_10
ORD IDord-0f2febcda39844b08827069bbb96b160
Source noteuspto-grants-1985_10