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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247174Generated: October 30, 2026

1-tert-butyl-2,4-dinitrobenzene → 4-(Tert-butyl)-3-nitroaniline

https://huagongshe.com/reaction/2247174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-butyl-2,4-dinitrobenzeneHCID 238590—
ReactantSulfurHCID 5362487—
SolventWaterHCID 962—
Product4-(Tert-butyl)-3-nitroanilineHCID 316163—

Reaction Steps

A mixture of 1,3-dinitro-4-tert-butylbenzene (10.0 g) in H2O (56 ml) was heated to reflux. A mixture of Na2S (21.42 g) and sulfur (2.85 g) in H2O (34 ml) was added over 1 h via an addition funnel. The reaction maintained at reflux for 1.5 h then cooled to RT and extracted with EtOAc. The organic extracts were combined and washed with H2O, brine, dried over MgSO4 and concentrated in vacuo to afford 4-tert-butyl-3-nitro-phenylamine which was used as is without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687643B2
Source datasetuspto-grants-2010_03
ORD IDord-c7d1eae810e04a66a4ac790a5cfacb77
Source noteuspto-grants-2010_03