HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Bromo-6-methoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
Reaction Steps
Sodium hydride (60%, 4.5 g, 112 mmol) was added in small portions to a mixture of 6-bromo-2-naphthol (25.0 g, 112 mmol), iodomethane (11.8 g, 168 mmol) and dimethylsulfoxide (150 ml). The mixture was stirred at room temperature overnight. Sodium hydroxide (200 ml, 1 M) was added, and the mixture was filtered. Yield 25.1 g, 95%. Mp 76-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680328B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-2e49379b15404ac9801784b308922460 |
| Source note | uspto-grants-2004_01 |