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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889239Generated: October 28, 2026

Benzyl Alcohol → 1-(Benzyloxy)-3-fluoro-2-nitrobenzene

https://huagongshe.com/reaction/889239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Difluoro-2-nitrobenzeneHCID 87922—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-3-fluoro-2-nitrobenzeneHCID 57834982—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1,3-difluoro-2-nitrobenzene (1.0 g, 6.29 mmol), benzyl alcohol (0.81 mL, 7.86 mmol) and potassium carbonate (1.74 g, 12.6 mmol) in DMF (5 mL) is heated at 60° C. for 18 h. The reaction mixture is poured into EtOAc, and washed with water and brine. The organic phase is concentrated and purified to give the title compound: 1H NMR (CDCl3) 7.36 (m, 6H), 6.83 (m, 2H), 5.20 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252820B2
Source datasetuspto-grants-2012_08
ORD IDord-19a3c7b7e2994e828b95d7cc43d3d618
Source noteuspto-grants-2012_08