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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | ((o-Methoxyphenoxy)methyl)oxirane | HCID 98357 | — |
| Reactant | HCID 20379505 | HCID 20379505 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 53872367 | HCID 53872367 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04181802 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-e75dca52ae4d4d3f959219322a00f5dc |
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| Source note | uspto-grants-1980_01 |
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