HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178521117, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178524538 | HCID 178524538 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178521117 | HCID 178521117 | — |
Reaction Steps
9.6 ml of thionyl chloride were added with stirring to a suspension of 8.75 g of the product of Step D in 285 ml of benzene and the mixture was refluxed for 90 minutes. Then, the benzene and excess thionyl chloride was evaporated and the residue was taken up twice in anhydrous benzene to obtain 2,8-bis-(trifluoromethyl)-4-hydroxy-3-quinoline-carboxylic acid chloride which was used as is for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04299831 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-bdd2dba9a4034d42b7eca19818958c64 |
| Source note | uspto-grants-1981_11 |