HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 71060073, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-4-(trifluoromethyl)benzoic acid | HCID 67605 | — |
| Reactant | Ethyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamido)propanoate | HCID 71059832 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71060073 | HCID 71060073 | — |
Reaction Steps
2-bromo-4-(trifluoromethyl)benzoic acid (538 mg, 2.0 mmol), ethyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamido)propanoate (1.0 g, 3.0 mmol), Pd(dppf)Cl2 (163 mg, 0.2 mmol), and K2CO3 (1.1 g, 8.0 mmol) were dissolved in 1,4-dioxane (12 mL) and water (4 mL) and heated to 90° C. After 3 h the resulting mixture was diluted EtOAc and water and 2N aqueous HCl was added until the pH of the aqueous layer was ca. 3-4. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried (Na2SO4) and concentrated to yield the title compound, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748624B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-fb8207f919204e38a7c980d7efdea2cc |
| Source note | uspto-grants-2014_06 |