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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309628Generated: November 1, 2026

Ethyl chloroformate → HCID 14012878, compound

https://huagongshe.com/reaction/2309628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 14012852HCID 14012852—
SolventTolueneHCID 1140—
ProductHCID 14012878HCID 1401287849.8%

Reaction Steps

To a stirred mixture of 72 parts of 1-(3-furanylmethyl)-2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazole and 324 parts of methylbenzene were added dropwise 25.5 parts of ethyl carbonochloridate at reflux. Upon completion, stirring was continued for 2 hours at reflux temperature. After cooling, the mixture was washed twice with a sodium hydroxide solution 5%, once with water, dried, filtered and evaporated. This residue, together with 560 parts of 2-propanol, 69.9 parts of potassium hydroxide and 6 parts of water, was stirred and refluxed for 22 hours. The whole was cooled and evaporated. The residue was taken up in water. The product was extracted three times with dichloromethane. The combined extracts were washed twice with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane, methanol and ammonium hydroxide (90:10:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was stirred in 2-propanone. The product was filtered off and dried, yielding 28.0 parts (49.8%) of 1-(3-furanylmethyl)-2-(4-piperidinylmethyl)-1H-benzimidazole; mp. 180° C. (73).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-1e311bf0251546b78eb849a6ffd06945
Source noteuspto-grants-1987_09