HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-Acetamino-4-acetoxy-1,2-benzisothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-Nitro-4-hydroxy-1,2-benzisothiazole | HCID 135765373 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 7-Acetamino-4-acetoxy-1,2-benzisothiazole | HCID 20349941 | 67% |
Reaction Steps
5.0 g of 7-nitro-4-hydroxy-1,2-benzisothiazole, in a mixture of 50 ml of acetic anhydride, 10 ml of acetic acid and 50 mg of a 5% strength palladium-on-charcoal catalyst, are left for 10 hours at 60° C. under 100 bars hydrogen pressure. After the mixture has cooled, the catalyst is filtered off, the filtrate is concentrated under reduced pressure and the partially crystalline crude product is recrystallized from acetic anhydride. 4.2 g (67% of theory) of 7-acetamino-4-acetoxy-1,2-benzisothiazole of melting point 215°-216° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189433 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-16499a6ed4064bd39bd7dfdcf0158228 |
| Source note | uspto-grants-1980_02 |