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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449689Generated: October 29, 2026

Phosphorus tribromide → 1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazole

https://huagongshe.com/reaction/449689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium BicarbonateHCID 516892—
Reactant(1-(2-bromoethyl)-3-nitro-1H-pyrazol-5-yl)methanolHCID 58043832—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazoleHCID 5750208367%

Reaction Steps

To a solution of (1-(2-bromoethyl)-3-nitro-1H-pyrazol-5-yl)methanol (4.24 g, 17.0 mmol) in chloroform (100 mL) was cooled to 0° C. was added phosphorus tribromide (4.59 g, 1.6 ml, 17.0 mmol) drop wise via syringe. The resulting solution was warmed to room temperature and stirred for 2 h. The resulting solution was cooled to 0° C. and diluted with dichloromethane (50 ml). The resulting solution was made basic (pH 8.5) with saturated aqueous sodium bicarbonate was (20 mL). The layers were separated, and the aqueous layer was extracted with dichloromethane (3×50 mL). The combined organic layers were washed with brine (30 mL), dried over magnesium sulfate. The resulting mixture was filtered and concentrated in vacuo and the residue purified by flash chromatography (silica gel, SF40-240 g, 15% to 40% ethyl acetate in hexanes) to give 1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazole (3.56 g, 67%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481540B2
Source datasetuspto-grants-2013_07
ORD IDord-568b6c27e832472ebdde4dcc01e42122
Source noteuspto-grants-2013_07