HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-BROMO-5-METHOXYNAPHTHALENE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromonaphthalen-1-ol | HCID 12336394 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-BROMO-5-METHOXYNAPHTHALENE | HCID 10900649 | 64% |
Reaction Steps
A suspension of 1-bromo-5-hydroxy-naphthalene (1.56 g, 7.0 mmol, prepared according to patent WO0146181), K2CO3 (1.45 g, 10.5 mmol), tetrabutylammonium chloride (15 mg, 0.05 mmol) and dimethyl sulfate (1.32 ml, 10.5 mmol) in MeCN was refluxed for 1 hour. After the addition of water, the aqueous phase was extracted three times with CH2Cl2. The combined organic layers were washed with water, dried over MgSO4, filtered and the solvent was removed under reduced to provide 1-bromo-5-methoxy-naphthalene (1.05 g, 64%) as a white solid, MS: m/e=236 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005432B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-1183b18990504a3fa1b3198d4d7d073f |
| Source note | uspto-grants-2006_02 |