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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450434Generated: November 1, 2026

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

https://huagongshe.com/reaction/450434

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 numberUS08486951B2
Source datasetuspto-grants-2013_07
ORD IDord-7bc41a100204499fba492195a50c09df
Source noteuspto-grants-2013_07