HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetonitrile → HCID 70979221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,3-Dibromopyridine | HCID 817102 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 70979221 | HCID 70979221 | — |
Reaction Steps
2,3-Dibromo-pyridine (1 eq., 0.5 g) and Phenyl-acetonitrile (4 eq., 0.97 mL) were mixed in NMP (3 mL). Potassium tert-butoxide (1.3 eq, 0.3 g) was added to the solution. The resulting mixture was heated in microwave at 110° C. for 40 min EtOAc and water were added to the reaction mixture. The aqueous layer was separated and extracted with EtOAc (×3). The combined organics were washed with brine, dried (MgSO4) and concentrated in vacuo to afford the title compound as a yellow solid. It was used in the next step without further purification
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975406B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c20c8f7598164ef797bfc7253dbc78fd |
| Source note | uspto-grants-2015_03 |