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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110496Generated: October 27, 2026

Water → 2,1,3-Benzothiadiazole, 4-methyl-5-nitro-

https://huagongshe.com/reaction/2110496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Methyl-2,1,3-benzothiadiazoleHCID 2781262—
ReactantSulfuric acid, mixt. with nitric acidHCID 71777668—
SolventSulfuric AcidHCID 1118—
Product2,1,3-Benzothiadiazole, 4-methyl-5-nitro-HCID 676446—
Product4-Methyl-7-nitrobenzo[1,2,5]thiadiazoleHCID 676447—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-methyl-benzo[1,2,5]thiadiazole (5.57 g, 37.1 mmol) in conc. H2SO4 (14.5 mL) at 0° C. was slowly added HNO3/H2SO4 (3.25 mL/4.25 mL). The reaction mixture was stirred at 0° C. for 20 min and then at rt for 30 min and then was poured into iced water (200 mL). The resulting precipitate was isolated by filtration, rinsed with water and purified by silica gel flash chomatography, eluting with CHCl3 to give compound 839B (1.5 g) as a yellow solid and 4-methyl-7-nitro-benzo[1,2,5]thiadiazole (2.0 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517904B2
Source datasetuspto-grants-2009_04
ORD IDord-4bd482dfa81b4038b5bfbc6833580f19
Source noteuspto-grants-2009_04