Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050246Generated: November 1, 2026

1-Bromo-3-chloropropane → HCID 20506304, compound

https://huagongshe.com/reaction/2050246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant2-cyclohexyl-1H-1,3-benzodiazoleHCID 37587—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTolueneHCID 1140—
ProductHCID 20506304HCID 20506304—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 20 parts of 2-cyclohexyl-1H-benzimidazole, 2 parts of N,N,N-triethylbenzenemethanaminium chloride, 225 parts of a sodium hydroxide solution 50% and 140 parts of tetrahydrofuran is stirred and heated to about 40° C. Then there are added 31.5 parts of 1-bromo-3-chloropropane and stirring is continued for 15 minutes at 60° C. The reaction mixture is cooled, methylbenzene is added and the layers are separated. The aqueous phase is extracted with methylbenzene. The combined methylbenzene-phases are washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 1-(3-chloropropyl)-2-cyclohexyl-1H-benzimidazole as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-a20b5bd5617e45089ef68ff9e8e9404c
Source noteuspto-grants-1980_04