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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377808Generated: November 1, 2026

2-Tert-Butylphenol → 1-tert-Butyl-2-(2-nitrophenoxy)benzene

https://huagongshe.com/reaction/2377808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-ButylphenolHCID 6923—
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product1-tert-Butyl-2-(2-nitrophenoxy)benzeneHCID 15415266122.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2-chloronitrobenzene (9.5 g, 60 mmol), 2-t-butyl phenol (9.04 g, 60.2 mmol) and potassium carbonate (10.6 g) in DMF was heated at 130° C. for 6 days. The reaction was cooled to rt and partitioned between diethyl ether (400 mL) and water (500 mL). The organic layer was separated and the aqueous layer was extracted with ether (3×100 mL). The combined organic layers were dried over magnesium sulfate, filtered and evaporated to give 1-tert-butyl-2-(2-nitrophenoxy)benzene (20 g). (M+H)+=216.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470712B2
Source datasetuspto-grants-2008_12
ORD IDord-54406fba48aa4b17b8c686b64e9d12a1
Source noteuspto-grants-2008_12