HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Phenylthio-5-trifluoromethylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Phenylthio)-5-(trifluoromethyl)benzonitrile | HCID 1489521 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Phenylthio-5-trifluoromethylbenzoic acid | HCID 104231 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
6 g of 2-(phenylthio)-5-trifluoromethyl-benzonitrile, 40 ml of 15% aqueous sodium hydroxide solution and 12 ml of ethanol are heated under reflux for 12 hours and then cooled. After the addition of 100 ml of water, the mixture is extracted with 80 ml of benzene. The aqueous phase is cooled to 0° C and acidified with concentrated hydrochloric acid. The precipitate which separates out is extracted with methylene chloride. The organic phase is washed with water until neutral, dried over sodium sulphate, filtered and evaporated. There is obtained 2-(phenylthio)-5-trifluoromethyl-benzoic acid which melts at 140°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006145 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-808760e5b6ba4c0c9333276f1be42940 |
| Source note | uspto-grants-1977_02 |