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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353698Generated: October 31, 2026

Ethanol → 5,7-Dimethyl-2,1,3-benzothiadiazol-4-amine

https://huagongshe.com/reaction/353698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium DithioniteHCID 24489—
Reactant5,7-Dimethyl-4-nitro-2,1,3-benzothiadiazoleHCID 23511539—
SolventWaterHCID 962—
Product5,7-Dimethyl-2,1,3-benzothiadiazol-4-amineHCID 12059958—

Reaction Steps

5,7-Dimethyl-4-nitro-2,1,3-benzothiadiazole (20 g) is warmed to ebullition in water (2.2 l) and ethanol (2.2 l) and sodium dithionite is added portionwise (strongly exothermic reaction). The reaction mixture is immediately cooled in an ice bath and extracted with ethyl acetate. The organic phase is concentrated by evaporation and the residue recrystallised in water to give 4-amino-5,7-dimethyl-2,1,3-benzothiadiazole. Mp=113-114°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756367B2
Source datasetuspto-grants-2004_06
ORD IDord-e5e7b9d1e022410698d2ae555157909d
Source noteuspto-grants-2004_06