HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-Benzyloxy-1-bromo-6-methoxy-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-6-methoxynaphthalen-2-ol | HCID 18428746 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Benzyloxy-1-bromo-6-methoxy-naphthalene | HCID 11702908 | 37.5% |
Reaction Steps
Add 1-bromo-6-methoxy-naphthalen-2-ol (66.7 g, 264 mmol), potassium carbonate (K2CO3, 40.0 g, 290 mmol) and benzyl bromide (49.6 g, 290 mmol) to DMF (800 mL). Stir the mixture at ambient temperature for 1 hour. Add water (400 mL) to precipitate the product. Collect the precipitate and wash the filter cake with heptane (3×125 mL) then dry to provide 2-benzyloxy-1-bromo-6-methoxy-naphthalene (83.7 g, 98.9 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476300B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-ce72f5b9b1ff4692a1324da43746eb77 |
| Source note | uspto-grants-2013_07 |