HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → 2-Chloro-4-(4-phenoxyphenyl)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 135741338 | HCID 135741338 | — |
| Product | 2-Chloro-4-(4-phenoxyphenyl)nicotinonitrile | HCID 86665678 | 90% |
Reaction Steps
Following conditions described in Step 1 of Example 3, 2-chloro-4-(4-hydroxyphenyl)nicotinonitrile was reacted with phenylboronic acid to give 2-chloro-4-(4-phenoxyphenyl)nicotinonitrile (60 mg, 90% yield). 1H NMR (500 MHz, CDCl3) 8 ppm 8.56 (1H, δ, J=5.22 Hz), 7.53-7.67 (2H, m), 7.37-7.49 (3H, m), 7.22 (1H, t, J=7.42 Hz), 7.09-7.16 (4H, m); MS (ES+) m/z: 307 (M+H); LC retention time: 3.863 min (analytical HPLC Method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846673B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-3621bb685b0e4d03bab60adf91c4dbd0 |
| Source note | uspto-grants-2014_09 |