HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178521116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178524537 | HCID 178524537 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178521116 | HCID 178521116 | 102.2% |
Reaction Steps
31.89 g of thionyl chloride were added to a suspension of 17.246 g of the product of Step E in 535 ml of anhydrous benzene and the mixture was refluxed for 105 minutes and was then evaporated to dryness under reduced pressure at 40° C. The residue was taken up in benzene and the solution was evaporated to dryness under the same conditions to obtain 18.62 g of 2,7-bis-(trifluoromethyl)-4-hydroxy-3-quinolinecarboxylic acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04299831 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-8d90c6882e3d4be498130a4b3c43c4cb |
| Source note | uspto-grants-1981_11 |