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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765123Generated: November 2, 2026

Phosphorus oxybromide → HCID 21106849, compound

https://huagongshe.com/reaction/1765123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
ReactantHCID 68709545HCID 68709545—
SolventChloroformHCID 6212—
ProductHCID 21106849HCID 2110684996.7%

Reaction Steps

2-(2,6-Difluorobenzyl)-1-hydroxy-1H-pyrazole (81.2 mg, 0.386 mmol, 1.0 eq) and 5 ml of anhydrous CHCl3 were combined in a flame-dried 25 mL round-bottom flask under argon and cooled in an ice/water bath. A solution of POBr3 (398.1 mg, 1.39 mmol, 3.60 eq) in 3 mL of CHCl3 was added using a syringe in aliquots over an hour period with stirring. The reaction solution was warmed to room temperature and stirred for 16 hours. The CHCl3 was removed in vacuo and the resulting orange mixture was neutralized with saturated aqueous NaHCO3 and extracted with 3×30 mL of diethyl ether. The combined ether fractions were washed with brine, dried over Na2SO4 and concentrated in vacuo to yield 101.5 mg (96.7% yield) of 5-bromo-1-(2,6-difluorobenzyl)-1H-pyrazole as a hygroscopic orange-tan colored solid. 1H NMR (CDCl3 300 MHz) δ 7.51 (d, 1H), 7.34 (m, 1H), 6.94 (t, 2H), 6.29 (d, 1H), 5.50 (s, 2H). LC/MS (ES) M+1=273.1, 275.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226930B2
Source datasetuspto-grants-2007_06
ORD IDord-106c3a35703c48dc8dca8a539439e47c
Source noteuspto-grants-2007_06