HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Benzyloxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester | HCID 59326573 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester | HCID 59326602 | 94% |
Reaction Steps
To a mixture of 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester (8.0 g, 34.2 mmol) and potassium carbonate (9.45 g, 68.4 mmol) was added benzyl bromide (4.5 mL, 37.6 mmol) in acetone (100 mL). The resulting mixture was vigorously stirred at reflux for 10 hours under a nitrogen atmosphere. The mixture was cooled and filtered. The combined organic solution was concentrated in vacuo to give 4-benzyloxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester (10.4 g, 94%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642629B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-fae345fd3ca24e94a92c9e1ca9a7d322 |
| Source note | uspto-grants-2014_02 |