HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178469127, compound → HCID 178524538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178469127 | HCID 178469127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178524538 | HCID 178524538 | 94.9% |
Reaction Steps
A solution of 61.1 g of the product of Step C in 900 ml of ethanol and 300 ml of 36° Be sodium hydroxide solution was refluxed for 7 hours and the ethanol was evaporated under reduced pressure. The mixture was poured into water and the mixture was extracted with ether. The ether phase was washed with water and the combined aqueous phases were acidified with hydrochloric acid and were iced and vacuum filtered. The recovered crystals were washed and dried to obtain 53.4 g of 2,8-bis-(trifluoromethyl)-4-hydroxy-3-quinoline-carboxylic acid melting at 188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04299831 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-9dd109afd3104231bc20a06ef5174686 |
| Source note | uspto-grants-1981_11 |