HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-[2-(2,4-di-tert-pentylphenoxy)-butyramido]-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 2-(2,4-Bis(1,1-dimethylpropyl)phenoxy)butyryl chloride | HCID 170393 | — |
| Reactant | 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-aminophenol | HCID 20531324 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-[2-(2,4-di-tert-pentylphenoxy)-butyramido]-phenol | HCID 20531321 | — |
Reaction Steps
A solution of 33.85 g (0.1 mole) of 2-(2,4-di-tert-pentylphenoxy)butyryl chloride in 80 ml of dioxan was added to a solution of 26.85 g (0.1 mole) of 2-(3-chloro-2,2,3-trifluoropropionamido)-5-aminophenol and 23.7 ml (0.2 mole) of quinoline in 500 ml of dioxan at room temperature. The mixture was stirred for 90 minutes and left standing overnight. Next it was poured out in 2 l of icewater and 100 ml of concentrated hydrochloric acid. The sticky residue was extracted with ether, rinsed with water until free from acid, and dried. The solvent was evaporated and the residue recrystallized from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04341864 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-a5866f60b69b4438a7eb715e4469aa46 |
| Source note | uspto-grants-1982_07 |