HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Isothiazolecarboxylic acid, 3-(3-(trifluoromethyl)phenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 3-(3-trifluoromethylphenyl)-5-isothiazolecarboxylate | HCID 13073224 | — |
| Reactant | 3-(3-Trifluoromethylphenyl)-5-isothiazolecarboxylate | HCID 86738545 | — |
| Product | 5-Isothiazolecarboxylic acid, 3-(3-(trifluoromethyl)phenyl)- | HCID 3067924 | 85% |
Reaction Steps
A solution of 1.6 g. of methyl 3-(3-trifluoromethylphenyl)-5-isothiazolecarboxylate in 30 ml. of 95% alcohol containing 1.0 g. of potassium hydroxide was heated at reflux for one hour. The reaction mixture then was added to 50 g. of ice, and the aqueous solution was acidified by the addition of 12 N aqueous hydrochloric acid. The product which precipitated was collected by filtration and crystallized from toluene and hexane to provide 1.3 g. of 3-(3-trifluoromethylphenyl)-5-isothiazolecarboxylate acid. Yield 85%. M.P. 162.5°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04346094 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-7997b32bf61d49c8a04a6b7b00f35295 |
| Source note | uspto-grants-1982_08 |