HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-6-methoxynaphthalene → 2-Methoxy-6-phenylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Product | 2-Methoxy-6-phenylnaphthalene | HCID 11253308 | — |
Reaction Steps
The title compound was prepared by reacting 2-bromo-6-methoxynaphthalene (1.97 g, 8.31 mmol) with phenylmagnesium bromide according to the method used to prepare intermedite 10 to yield 1.59 g (82%) of a white solid: mp 122–126° C.; 1H NMR (CDCl3): δ 3.94 (3H, s), 7.16–7.18 (2H, m), 7.34–7.37 (1H, m), 7.46–7.49 (2H, m), 7.69–7.72 (2H, m), 7.78–7.82 (2H, m), 7.97 (1H, t); MS (El) m/z 234.2 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067524B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-22b921d20dc4438e9a443a2d080ffc07 |
| Source note | uspto-grants-2006_06 |