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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711652Generated: October 31, 2026

Benzyl Alcohol → 1-(Benzyloxy)-2,3-difluoro-4-nitrobenzene

https://huagongshe.com/reaction/1711652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2,3-Trifluoro-4-nitrobenzeneHCID 69871—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-2,3-difluoro-4-nitrobenzeneHCID 5747087736%

Reaction Steps

A solution of 1,2,3-trifluoro-4-nitro-benzene (30 g, 0.17 mol) and benzyl alcohol (18.4 g, 0.17 mol) in DMF (300 mL) was treated with K2CO3 (35 g, 0.25 mol) and the resulting mixture was stirred at RT for 8 h. Water (300 mL) was added, and the mixture was extracted with EtOAc (3×500 mL). The combined organics were washed with brine, dried (MgSO4), concentrated in vacuo and chromatographed on silica gel to give 1-benzyloxy-2,3-difluoro-4-nitrobenzene (16 g, 36% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.06 (m, 1H), 7.49-7.30 (m, 6H), 5.37 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790756B2
Source datasetuspto-grants-2010_09
ORD IDord-fdb3a152b7604536b8db6358c6ea7bea
Source noteuspto-grants-2010_09