Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 86719510 | HCID 86719510 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86719509 | HCID 86719509 | 69% |
Reaction Steps
To a solution of 7-methoxy-1-(trifluoromethyl)naphthalen-2-amine (2 g, 8.29 mmol) in dichloromethane (20 ml) was added dropwise BBr3 (4 ml, 42 mmol, 5 eq.) with stirring at −78° C. The resulting solution was stirred overnight at room temperature and then quenched by ice—water (50 ml) and extracted with dichloromethane (3×50 ml). The combined organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to afford 7-amino-8-(trifluoromethyl)naphthalen-2-ol as a brown solid (1.3 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249102B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-58886016d3434319b749ecdc7c8d6527 |
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| Source note | uspto-grants-2016_02 |
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