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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060660Generated: November 2, 2026

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

https://huagongshe.com/reaction/2060660

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

1,2,3-Trifluoro-4-nitrobenzene (30 g, 0.17 mol), benzyl alcohol (18.4 g, 0.17 mol) and K2CO3 (35 g, 0.25 mol) were combined in DMF (300 mL) and were stirred at RT for 8 h. Water (300 mL) was added, and the mixture was extracted with EtOAc (3×500 mL). The combined organic layers were washed with brine, dried (MgSO4), concentrated in vacuo and purified by column chromatography 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 numberUS08278331B2
Source datasetuspto-grants-2012_10
ORD IDord-29603b53910c4c2c8e949cd4b3111a7e
Source noteuspto-grants-2012_10