HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-6-methoxynaphthalene → 2-Methoxy-6-(3-methoxyphenyl)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | (3-Methoxyphenyl)boronic acid | HCID 2734370 | — |
| Product | 2-Methoxy-6-(3-methoxyphenyl)naphthalene | HCID 11402834 | — |
Reaction Steps
The title compound was prepared by reacting 6-methoxy-2-bromonaphthalene (3.99 g, 13.0 mmol) with 3-methoxyphenylboronic acid (2.18 g, 14.3 mmol according to method A to yield 1.18 g (34%) of a white solid: mp 80° C.; 1H NMR (CDCl3): δ 3.88 (3H, s), 3.92(3H, s), 6.90 (1H, dd, J=2.17 Hz, J=7.76 Hz), 7.14–7.18 (2H, m), 7.22–7.24 (1H, m), 7.28 (1H, d, J=7.45 Hz), 7.36–7.39, (1H, m), 7.70 (1H, dd, J=1.86 Hz, J=8.70 Hz), 7.77–7.80 (2H, m), 7.96 (1H, d, J=1.24 Hz); MS (ESI) m/z 265 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067524B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-33d6edc40fd54bdcb358f51dc7c49a1a |
| Source note | uspto-grants-2006_06 |