HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoro-4-methoxyphenylboronic acid → 3-(3-Fluoro-4-methoxyphenyl)-7-hydroxy-1-naphthonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoro-4-methoxyphenylboronic acid | HCID 2782194 | — |
| Reactant | 3-Bromo-7-hydroxy-1-naphthonitrile | HCID 11322598 | — |
| Product | 3-(3-Fluoro-4-methoxyphenyl)-7-hydroxy-1-naphthonitrile | HCID 11737917 | — |
Reaction Steps
The title compound was prepared by reacting 3-bromo-7-hydroxy-1-naphthonitrile (0.208 g, 0.839 mmol) with 3-fluoro-4-methoxyphenylboronic acid (0.18 g, 1.1 mmol) according to method A to yield 0.16 (65%) of a light yellow solid. An analytical sample was prepared by preparative reverse phase HPLC to yield the title compound as a white solid: mp 214-216° C.; 1H NMR (DMSO-d6): δ 3.90 (3H, s), 7.23-7.32 (2H, m), 7.37 (1H, d, J=2.24 Hz), 7.65-7.70 (1H, m), 7.79 (1H, dd, J=2.22 Hz, J=13.10 Hz), 8.03 (1H, d, J=8.96 Hz), 8.41 (1H, d, J=1.86 Hz), 8.50 (1H, d, J=1.43 Hz), 10.55 (1H, s); MS (ESI) m/z292 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06914074B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-4ebee11452804ad28a768e6f95a59cd1 |
| Source note | uspto-grants-2005_07 |