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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413452Generated: November 3, 2026

1-Bromo-3-chloropropane → 3-(3-chloropropyl)-1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1413452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
Reactant1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-oneHCID 20506287—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Product3-(3-chloropropyl)-1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-oneHCID 20506315—

Reaction Steps

To a stirred and hot (±50° C.) mixture of 34 parts of 1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-one, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 300 parts of a sodium hydroxide solution 50% are added 57 parts of 1-bromo-3-chloropropane (exothermic reaction: temperature rises to 70° C.). The whole is stirred for one hour at 65°-70° C. The reaction mixture is cooled and poured onto crushed ice. The product is extracted with methylbenzene. The extract is washed three times with water, dried, filtered and evaporated. The oily residue is distilled, yielding 3-(3-chloropropyl)-1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-one; bp. 140° C. at 0.02 mm. pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250176
Source datasetuspto-grants-1981_02
ORD IDord-d8b992fd73554a35a11e404ed0c573fb
Source noteuspto-grants-1981_02