HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[(trifluoromethyl)thio]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21439338 | HCID 21439338 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(trifluoromethyl)thio]benzoic acid | HCID 2777853 | — |
Reaction Steps
A solution of 5.0 g. of ethyl-o-(trifluoromethylthio)benzoate, 30 ml. of ethanol and 20 ml. of 10% sodium hydroxide was refluxed for 1.5 hrs. After cooling, the solution was acidified with 6N hydrochloric acid. The product was collected by filtration, dried, and recrystallized from a mixture of 60% hexane-40% benzene to give o-(trifluoromethylthio)benzoic acid, m.p. 119°-121° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020169 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-fe42694234264620a018a45ad173d911 |
| Source note | uspto-grants-1977_04 |