HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5,7-Dimethyl-2,1,3-benzothiadiazol-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 5,7-Dimethyl-4-nitro-2,1,3-benzothiadiazole | HCID 23511539 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,7-Dimethyl-2,1,3-benzothiadiazol-4-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756367B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-e5e7b9d1e022410698d2ae555157909d |
| Source note | uspto-grants-2004_06 |