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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113693Generated: November 1, 2026

2-(Bromomethyl)-1,3-difluorobenzene → HCID 68709545, compound

https://huagongshe.com/reaction/2113693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)-1,3-difluorobenzeneHCID 581435—
Reactant1-hydroxy-1H-pyrazoleHCID 3016733—
SolventChloroformHCID 6212—
ProductHCID 68709545HCID 6870954570.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-Hydroxypyrazole (49.3 mg, 0.59 mmol, 1.0 eq) was mixed with 165.8 mg (0.80 mmol, 1.36 eq) of 2,6-difluorobenzyl bromide in ˜1-2 mL of anhydrous CHCl3 under argon. The mixture was heated at 80° C. for 18 h under inert atmosphere in a sealed flask without condenser. The residue was partitioned between 37 weight percent aqueous HCl and toluene. The aqueous layer was collected and the toluene fraction extracted again with 37 weight percent aqueous HCl. The combined aqueous HCL fractions were neutralized with 5N aqueous NaOH to pH˜11-12 and then back-extracted with 3×30 mL of CHCl3. The organic layers were combined, washed with brine, dried over Na2SO4 and concentrated under reduced pressure to yield 86.3 mg (70.1% yield) of 2-(2,6-difluorobenzyl)-1-hydroxy-1H-pyrazole as a tan brown solid. 1H NMR (CDCl3 300 MHz) δ 7.37 (m, 1H), 7.18 (d, 1H), 6.95 (t, 2H), 6.85 (d, 1H), 6.11 (t, 1H), 5.43 (s, 2.00 H). LC/MS (ES) M+1=211.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432266B2
Source datasetuspto-grants-2008_10
ORD IDord-70dc44f1f15e433f90ab7dccac050fd8
Source noteuspto-grants-2008_10