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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555410Generated: November 1, 2026

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

https://huagongshe.com/reaction/555410

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 numberUS08053450B2
Source datasetuspto-grants-2011_11
ORD IDord-75ffc190597c45b0bd966b0bc5309c5f
Source noteuspto-grants-2011_11