Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258836Generated: November 1, 2026

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

https://huagongshe.com/reaction/258836

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 2050631584%

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 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 1 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 40 parts (84%) of 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 numberUS04035369
Source datasetuspto-grants-1977_07
ORD IDord-26ddc991bee84baea5c9d9e2a5c411f3
Source noteuspto-grants-1977_07