HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15070158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Trifluoromethyl)anilinium chloride | HCID 2723961 | — |
| Reactant | HCID 13389070 | HCID 13389070 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15070158 | HCID 15070158 | — |
Reaction Steps
A solution of the 2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propionyl chloride (prepared in Step A) in 50 ml of acetonitrile was added to a mixture of 3.82 g (19.4 mmol) of 4-aminobenzotrifluoride, hydrochloride and 4.90 g (48.4 mmol) of triethylamine in 25 ml of acetonitrile. The reaction mixture was warmed at reflux for 4.0 hours and then poured over crushed ice. The resulting precipitate was collected by filtration and dried. The residual solid was recrystallized from methylcyclohexane to give 9.1 g (93 percent of theoretical) of the above-named product as a tan solid which melted at 140°-143° C. The structure of the product was confirmed by its IR and NMR spectrum. (Compound 1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04968343 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-b29a166c5946459a88b3e8dfa6243f90 |
| Source note | uspto-grants-1990_11 |