HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1,2-Benzisothiazol-4-ol, 7-amino-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-Acetamino-4-acetoxy-1,2-benzisothiazole | HCID 20349941 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 1,2-Benzisothiazol-4-ol, 7-amino- | HCID 135617187 | — |
Reaction Steps
This reduction is as a rule carried out under atmospheric pressure or in a closed vessel under superatmospheric pressure, with or without simultaneous heating. The reaction may be carried out in the presence of a diluent or solvent, for example, a lower alcohol, e.g. methanol, ethanol or preferably propanol, or in the acid required for the reduction, preferably in acetic acid, or in the acylating reaction medium of acetic acid and acetic anhydride, described above, in which 7-acetamino-4-acetoxy-1,2-benzisothiazole is obtained. 7-Acetamino-4-acetoxy-1,2-benzisothiazole can subsequently be deacylated in the above manner to give 7-amino-4-hydroxy-1,2-benzisothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189433 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-38f6917caac942a9a95e10acc735d2e3 |
| Source note | uspto-grants-1980_02 |