HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Fluoro-6-(phenylthio)-phenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12232352 | HCID 12232352 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Fluoro-6-(phenylthio)-phenylacetic acid | HCID 12232355 | — |
Reaction Steps
80 g of 3-fluoro-6-(phenylthio)-phenylacetonitrile, 225 ml of ethanol, 75.5 g of potassium hydroxide and 225 ml of water are heated under reflux for 9 hours. The ethanol is subsequently evaporated off under reflux and the residue treated with water until completely dissolved, whereafter the neutral constituents are extracted with benzene. The aqueous solution is acidified with concentrated hydrochloric acid and extracted with chloroform. The organic phase is washed with water, dried over sodium sulphate and evaporated under reduced pressure. There is obtained 3-fluoro-6-(phenylthio)-phenylacetic acid which melts at 80°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006144 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-8051ab67dee0478abf4d9dd1648cb3a9 |
| Source note | uspto-grants-1977_02 |