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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132589Generated: October 26, 2026

2-Nitrophenol → 1-(Benzhydryloxy)-2-nitrobenzene

https://huagongshe.com/reaction/132589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantPotassium CarbonateHCID 11430—
ReactantBromodiphenylmethaneHCID 236603—
ReactantPotassiumHCID 5462222—
SolventAcetoneHCID 180—
Product1-(Benzhydryloxy)-2-nitrobenzeneHCID 743412239.5%

Reaction Steps

A mixture of o-nitrophenol (2.08 g, 15.0 mmol), 1-[bromo(phenyl)methyl]benzene (3.70 g, 15.0 mmol) and potassium carbonated (K2CO3) (4.14 g, 30.0 mmol) in acetone (60 mL) was kept at reflux temperature for 5 h. The reaction mixture was cooled to room temperature, concentrated in vacuo. The residue was partitioned between dichloromethane (CH2Cl2) and water (H2O), organic layer dried over sodium sulphate (Na2SO4), filtered, concentrated. The residue was purified by silica gel flash chromatography to give subtitled compound (1.81 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388020B2
Source datasetuspto-grants-2008_06
ORD IDord-079031298525448db5b6e52e03b4a7e2
Source noteuspto-grants-2008_06