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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482617Generated: November 1, 2026

1-Bromo-3-chloropropane → 6-cyano-1-(3-chloropropyl)-1H-benzopyrazole

https://huagongshe.com/reaction/1482617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
Reactant1H-indazole-6-carbonitrileHCID 422529—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product6-cyano-1-(3-chloropropyl)-1H-benzopyrazoleHCID 11838693263.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

6-cyano-1H-benzopyrazole (14.3 g, 0.10 mol) was dissolved into 200 ml of 20% wt. sodium hydroxide, 3-chlorobromopropane (31.2 g, 0.20 mol) and tetrabutyl ammonium bromide (1.0 g) were added, and mixed for 5 min. The mixture was heated to 60° C., stirred to react 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 to produce 13.9 g of 6-cyano-1-(3-chloropropyl)-1H-benzopyrazole, with a yield of 63.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415047B2
Source datasetuspto-grants-2016_08
ORD IDord-daf1b395b3ef449a9238e19ab0b74f67
Source noteuspto-grants-2016_08