HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boric Acid → Methyl 2-(2,3'-dicyano-4'-hydroxybiphenyl-4-yl)isonicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | HCID 66995426 | HCID 66995426 | — |
| Reactant | Methyl 2-(3-cyano-4-([(trifluoromethyl)sulfonyl]oxy)phenyl)isonicotinate | HCID 86616562 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(2,3'-dicyano-4'-hydroxybiphenyl-4-yl)isonicotinate | HCID 136407394 | 47.5% |
Reaction Steps
1.32 g of methyl 2-[4′-(benzyloxy)-2,3′-dicyanobiphenyl-4-yl]isonicotinate, which had been obtained in the same manner as in Example 1(1) using 4-(benzyloxy)-3-cyanophenyl]boric acid and methyl 2-(3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)isonicotinate, was dissolved in a mixture of 50 ml of THF and 50 ml of methanol, and 0.5 g of palladium-carbon was added, followed by stirring in a hydrogen atmosphere at room temperature for 12 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure to obtain 0.5 g of methyl 2-(2,3′-dicyano-4′-hydroxybiphenyl-4-yl)isonicotinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816558B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-b45cfd19bb044b21b25a77e3294476a9 |
| Source note | uspto-grants-2010_10 |