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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337301Generated: October 29, 2026

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

https://huagongshe.com/reaction/337301

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 5750208367.3%

Reaction Steps

To as solution of (1-(2-bromoethyl)-3-nitro-1H-pyrazol-5-yl)methanol (4.24 g, 17 mmol) in chloroform (100 mL), cooled to 0° C., was added phosphorus tribromide (4.59 g, 1.6 mL, 17 mmol) drop wise. 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. The crude material was purified by flash chromatography (silica gel, SF40-240 g, 15% to 40% EtOAc in hexanes) to give 1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazole (3.58 g, 67%) as a white solid. 1H NMR (300 MHz, DMSO-d6) 8 ppm 3.92 (t, J=6.23 Hz, 2 H) 4.69 (t, J=6.23 Hz, 2 H) 4.89 (s, 2 H) 7.19 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889682B2
Source datasetuspto-grants-2014_11
ORD IDord-2a4d2659462a49c5b000d0b46cb7b7bd
Source noteuspto-grants-2014_11