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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377010Generated: October 26, 2026

2-Nitrophenol → 4-tert-Butyl-2,6-dinitroanisole

https://huagongshe.com/reaction/1377010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
Reactant4-tert-Butyl-2,6-dinitrophenolHCID 20042—
ReactantButralinHCID 36565—
ReactantMethyl iodide potassium carbonateHCID 86747754—
Product4-tert-Butyl-2,6-dinitroanisoleHCID 4252602—

Reaction Steps

An alternative synthesis for N-sec-butyl-4-tert-butyl-2,6-dinitroaniline is set forth in U.S. Pat. Nos. 4,289,907 and 4,395,572 to Chan. The starting material in this synthesis is a nitrophenol such as 2,6-dinitro-4-tert-butylphenol. The nitrophenol is methylated by reaction with methyl iodide/potassium carbonate to produce 4-tert-butyl-2,6-dinitroanisole. The 4-tert-butyl-2,6-dinitroanisole is then reacted with sec-butylamine to produce N-sec-butyl-4-tert-butyl-2,6-dinitroaniline. While effective in producing the desired product, this process also suffers from a number of distinct disadvantages.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663441
Source datasetuspto-grants-1997_09
ORD IDord-f92da87f7de34fbf9a06d53824d05a63
Source noteuspto-grants-1997_09