HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-Amino-4-benzyloxy-1,2-benzisothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Nitro-4-benzyloxy-1,2-benzisothiazole | HCID 20349942 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 7-Amino-4-benzyloxy-1,2-benzisothiazole | HCID 20349935 | 100% |
Reaction Steps
28.6 g of 7-nitro-4-benzyloxy-1,2-benzisothiazole are added in portions to a boiling mixture of 67 ml of water, 30 g of iron powder, 3 ml of glacial acetic acid and 167 ml of n-propanol and the mixture is then refluxed for a further hour. When it has cooled, it is neutralized with concentrated ammonia solution and filtered. The filter residue is washed with methylene chloride and the combined wash solutions are dried over magnesium sulfate and freed from the solvent under reduced pressure. 25.1 g (100% of theory) of 7-amino-4-benzyloxy-1,2-benzisothiazole of melting point 126°-128° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189433 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-d0ff86413b954b0d97b5004a7967a224 |
| Source note | uspto-grants-1980_02 |