Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916286Generated: October 27, 2026

Dimethyl Sulfoxide → 2-Amino-4-methyl-3,5-dinitrobenzonitrile

https://huagongshe.com/reaction/916286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant4-Amino-1,2,4-triazoleHCID 11432—
Reactant4-Methyl-3,5-dinitrobenzonitrileHCID 5134316—
Reactant2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
SolventAcetic AcidHCID 176—
Product2-Amino-4-methyl-3,5-dinitrobenzonitrileHCID 16726789—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

A solution of 4-methyl-3,5-dinitrobenzonitrile (10.5 kg; preparation see U.S. Pat. No. 3,162,675), 4-amino-4H-1,2,4-triazole (17.0 kg) and dimethyl sulfoxide (68.6 kg) was dosed into a mixture of lithium tert-butoxide (12.2 kg) and dimethyl sulfoxide (106.6 kg) over about 50 min, while maintaining the temperature of each solution at 20-25° C. After aging at 20-25° C. for about 2 h, acetic acid (8.9 kg) was dosed into the reaction mixture at about 20° C. over about 10 min. The product was crystallized by dosing water (158 L) into the reaction mixture over about 1.5 h at about 20° C. The product slurry was cooled to 10-15° C. and held at this temperature for about 45 min. The resultant slurry was filtered, and washed with water (106 L). The wet cake obtained was dried in a vacuum tray dryer at about 50° C. and 30 Torr to provide 2-amino-4-methyl-3,5-dinitrobenzonitrile as an orange-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268255B2
Source datasetuspto-grants-2007_09
ORD IDord-f81f1ace4ad44ce2b43f29a998567d05
Source noteuspto-grants-2007_09