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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198560Generated: October 26, 2026

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

https://huagongshe.com/reaction/1198560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantPotassium CarbonateHCID 11430—
ReactantBromodiphenylmethaneHCID 236603—
SolventAcetoneHCID 180—
Product1-(Benzhydryloxy)-2-nitrobenzeneHCID 7434122—

Reaction Steps

2-Nitrophenol (11.0 g, 79 mmole), anhydrous potassium carbonate (17.6 g, 127.4 mmole) and benzhydryl bromide (19.6 g, 79 mmol) in acetone (220 ml) were refluxed under nitrogen for 5 hours. The mixture was cooled, filtered and evaporated in vacuo. The residue was triturated with diethyl ether, filtered and evaporated. Trituration with 60°-80° C. petroleum ether yielded a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281593
Source datasetuspto-grants-1994_01
ORD IDord-bf579edc0ce849fe8869e66392514941
Source noteuspto-grants-1994_01