Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Methoxy-1-phenylnaphthalene | HCID 11322266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Phenylnaphthalen-2-ol | HCID 11218282 | 81.8% |
Reaction Steps
In methylene chloride (300 mL), dissolved was 2-methoxy-1-phenylnaphthalene (13.0 g, 55.5 mmol), and 670 mL of boron tribromide solution (1 M in methylene chloride) was added dropwise thereto at −78° C. Reaction was carried out for 3 hours while slowly raising the temperature to ambient temperature. When the reaction was completed, mixture of ice (150 g) and diethyl ether (250 mL) was added thereto. After isolating the organic layer, the aqueous layer was extracted with diethyl ether. The combined organic layer was dried over magnesium sulfate, and evaporated to remove the volatiles. The residue was purified via silica gel column chromatography by using mixed solvent of hexane and methylene chloride to obtain 1-phenylnaphthalen-2-ol (10.0 g, yield: 81.8%) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067511B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b8ea0ded6ffb4822898b5ea482c2e34f |
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| Source note | uspto-grants-2011_11 |
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