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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449673Generated: October 29, 2026

Phosphorus tribromide → 5-(Bromomethyl)-1-methyl-3-nitro-1H-pyrazole

https://huagongshe.com/reaction/449673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium BicarbonateHCID 516892—
Reactant(1-methyl-3-nitro-1H-pyrazol-5-yl)methanolHCID 50896828—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product5-(Bromomethyl)-1-methyl-3-nitro-1H-pyrazoleHCID 5854035663%

Reaction Steps

To a solution of (1-methyl-3-nitro-1H-pyrazol-5-yl)methanol (496 mg, 3.16 mmol) in chloroform (10 mL) at 0° C. was added phosphorus tribromide (854 mg, 0.30 mL, 3.16 mmol) drop wise via syringe. The resulting solution was warmed to room temperature and stirred for 1 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 (20 mL). The layers were separated, and the aqueous layer was extracted with dichloromethane (3×20 mL). The combined organic layers were dried over magnesium sulfate. The resulting mixture was filtered and concentrated in vacuo and the residue purified by flash chromatography (silica gel, 40 g, 20% to 40% ethyl acetate in hexanes) to give 5-(bromomethyl)-1-methyl-3-nitro-1H-pyrazole (436 mg, 63%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481540B2
Source datasetuspto-grants-2013_07
ORD IDord-2a746e58ff6c4d01a4508342611598c8
Source noteuspto-grants-2013_07