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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482595Generated: October 31, 2026

1-Bromo-3-chloropropane → 1-(3-chloropropyl)-1H-1,2,3-benzotriazole

https://huagongshe.com/reaction/1482595

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418385HCID 178418385—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product1-(3-chloropropyl)-1H-1,2,3-benzotriazoleHCID 524393880%

Reaction Conditions

Temperature60 °C

Reaction Steps

Benzotriazole (11.9 g, 0.10 mol) is dissolved into 100 ml of 30% wt. sodium hydroxide, 3-chlorobromopropane (30.2 g, 0.20 mol), tetrabutyl ammonium bromide (0.8 g) are added, and mixed for 5 min. The reaction solution is gradually heated to 60° C., stirred for reaction for 2 hours. Then the reaction solution was cooled down to ambient temperature, 100 ml of dichloromethane was added for extraction and liquid separation. To the aqueous phase, 100 of dichloromethane was added for extraction. Organic phases were mixed, washed with 100 ml of saturated saline. Liquid was separated, and organic phase was evaporated to dryness to produce oily product. Oily products were separated and purified by chromatography with neutral Al2O3, and eluted with dichlormethane to produce 15.6 g of 1-(3-chloropropyl)-1H-benzotriazole, with a yield of 80.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415047B2
Source datasetuspto-grants-2016_08
ORD IDord-85663a87dc774433930e5fa62d268dac
Source noteuspto-grants-2016_08