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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050245Generated: October 25, 2026

1-Bromo-3-chloropropane → 1-(3-chloropropyl)-2-methyl-1H-benzimidazole

https://huagongshe.com/reaction/2050245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
Reactant2-MethylbenzimidazoleHCID 11984—
ReactantSodium HydroxideHCID 14798—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Product1-(3-chloropropyl)-2-methyl-1H-benzimidazoleHCID 21239360—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred mixture of 13.2 parts of 2-methyl-1H-benzimidazole, 2 parts of N,N,N-triethylbenzenemethanaminium chloride and 150 parts of a sodium hydroxide solution 60% are added 30 parts of 1-bromo-3-chloropropane. To start the reaction, the whole is heated to about 40° C., whereupon the temperature rises to 50° C. (exothermic reaction). Stirring at about 50° C. is continued for 30 minutes. The reaction mixture is poured onto water and the product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 1-(3-chloropropyl)-2-methyl-1H-benzimidazole as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-fbf5ed9553b24a02bac8897dcafa0882
Source noteuspto-grants-1980_04