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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450424Generated: October 29, 2026

Benzyl Alcohol → 1-(Benzyloxy)-3-fluoro-2-methyl-4-nitrobenzene

https://huagongshe.com/reaction/450424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Difluoro-3-nitrotolueneHCID 12795486—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-3-fluoro-2-methyl-4-nitrobenzeneHCID 6672901833.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

1,3-Difluoro-2-methyl-4-nitro-benzene (16 g, 0.092 mol), benzyl alcohol (10 g, 0.092 mol) and K2CO3 (25.3 g, 0.18 mol), were combined in DMF (300 mL) and heated to 100° C. overnight. The mixture was poured into water and extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with brine, dried (Na2SO4), concentrated in vacuo and purified by silica gel chromatography to give 1-benzyloxy-3-fluoro-2-methyl-4-nitro-benzene (8 g, 33% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.04 (t, J=8.8 Hz, 1H), 7.30-7.46 (m, 5H), 7.08 (d, J=9.2 Hz, 1H), 5.28 (s, 2H), 2.13 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486951B2
Source datasetuspto-grants-2013_07
ORD IDord-1a9f2c02e07b4155bee276357e63c883
Source noteuspto-grants-2013_07