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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060680Generated: October 31, 2026

Benzyl Alcohol → 2-(Benzyloxy)-1,3-difluoro-5-nitrobenzene

https://huagongshe.com/reaction/2060680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2,3-Trifluoro-5-nitrobenzeneHCID 2782793—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-1,3-difluoro-5-nitrobenzeneHCID 2313034271%

Reaction Steps

Potassium carbonate (7.8 g, 56.4 mmol) was added to a solution of 1,2,3-trifluoro-5-nitrobenzene (5 g, 28.2 mmol) and benzyl alcohol (3.2 g, 29.6 mmol) in N,N-dimethylformamide (70 mL). The resultant mixture was stirred at RT overnight. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried (Na2SO4), concentrated under reduced pressure and purified by column chromatography to give 2-(benzyloxy)-1,3-difluoro-5-nitrobenzene (5.3 g, 71% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.15 (d, J=8.4 Hz, 2H), 7.46-7.37 (m, 5H), 5.39 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278331B2
Source datasetuspto-grants-2012_10
ORD IDord-dc062f852183491bb09eeda8d397dded
Source noteuspto-grants-2012_10