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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444475Generated: October 29, 2026

Chloroethane → HCID 12875760, compound

https://huagongshe.com/reaction/444475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroethaneHCID 6337—
ReactantSodium CarbonateHCID 10340—
Reactant1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
ReactantHCID 131712197HCID 131712197—
CatalystSodium IodideHCID 5238—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 12875760HCID 12875760107.7%

Reaction Steps

A suspension of 6.87 g of 3,4-dihydroxyphenyl chloromethylketone (trade product) and 8 g of 4-(2-oxobenzimidazolin-1-yl)piperidine (trade product), M.P. 183°-185° C., in 640 ml of methylethyl ketone, in the presence of 1.95 g of dried sodium carbonate and 0.1 g of sodium iodide, was refluxed for 12 hours. After the completion of the reaction, the precipitate was filtered off and washed with water. After drying, there were obtained 14 g of raw base which is transformed in hydrochloride in methanol by addition of hydrochloric ether. There were obtained 8 g of 1-(3,4-dihydroxy phenacyl)-4-(2-oxobenzimidazolin-1-yl)piperidine hydrochloride, white crystals melting at 310°-313° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264613
Source datasetuspto-grants-1981_04
ORD IDord-e15e5995276f4fe89dd59790964cf37c
Source noteuspto-grants-1981_04