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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696602Generated: November 4, 2026

4-Nitrophenol → p-(Benzyloxy)nitrobenzene

https://huagongshe.com/reaction/1696602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Productp-(Benzyloxy)nitrobenzeneHCID 7084290.4%

Reaction Steps

To a mixture of 4-nitrophenol (10.0 g, 71.9 mmol), K2CO3 (19.9 g, 143.9 mmol) and KI (2.6 g, 15.8 mmol) in acetonitrile was added chloromethylbenzene (10.0 g, 79.1 mmol) at RT. The resultant mixture was heated to reflux for 3 h. After removal of the solvent, the residue was dissolved in EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated to afford 4-benzyloxynitrobenzene (14.9 g, 90% yield). 1H NMR (400 MHz, CDCl3): δ 8.20 (d, J=8.0 Hz, 2H), 7.43-7.37 (m, 5H), 7.03 (d, J=8.0 Hz, 2H), 5.17 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163756B2
Source datasetuspto-grants-2012_04
ORD IDord-0d8b7bda83b34bc29e6c6588ac65edb6
Source noteuspto-grants-2012_04