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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051690Generated: October 31, 2026

((o-Methoxyphenoxy)methyl)oxirane → HCID 53872367, compound

https://huagongshe.com/reaction/2051690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((o-Methoxyphenoxy)methyl)oxiraneHCID 98357—
ReactantHCID 20379505HCID 20379505—
SolventIsopropanolHCID 3776—
ProductHCID 53872367HCID 5387236728%

Reaction Steps

A mixture of 4 parts of [(2-methoxyphenoxy)methyl]oxirane, 5.3 parts of 6-chloro-1,3-dihydro-1-(3-piperidinylmethyl)-2H-benzimidazol-2-one and 120 parts of 2-propanol is stirred and refluxed for 5 hours. The reaction mixture is cooled and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone and 2,2'-oxybispropane. The product is filtered off and crystallized from 4-methyl-2-pentanone, yielding 2.5 parts (28%) of 6-chloro-1,3-dihydro-1-{1-[2-hydroxy-3-(2-methoxyphenoxy)propyl]-3-piperidinylmethyl}-2H-benzimidazol-2-one; mp. 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181802
Source datasetuspto-grants-1980_01
ORD IDord-e75dca52ae4d4d3f959219322a00f5dc
Source noteuspto-grants-1980_01