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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449681Generated: October 29, 2026

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

https://huagongshe.com/reaction/449681

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 5750208378%

Reaction Steps

To as solution of (1-(2-bromoethyl)-3-nitro-1H-pyrazol-5-yl)methanol (482 mg, 1.93 mmol) in chloroform (20 mL) was cooled to 0° C. was added phosphorus tribromide (522 mg, 0.18 mL, 1.93 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 was (20 mL). The layers were separated, and the aqueous layer was extracted with dichloromethane (3×20 mL). The combined organic layers were washed with brine (30 mL), dried over magnesium sulfate. The resulting mixture was filtered and concentrated in vacuo to give 1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazole (469 mg, 78%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481540B2
Source datasetuspto-grants-2013_07
ORD IDord-ff102a4427ff4573a488bc04a45c2110
Source noteuspto-grants-2013_07