HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288907Generated: October 30, 2026
Hydrogen Bromide → 1-Hydroxy-5-phenoxynaphthalene
https://huagongshe.com/reaction/2288907
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-Methoxy-5-phenoxynaphthalene | HCID 18702041 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Hydroxy-5-phenoxynaphthalene | HCID 18702040 | 60.1% |
Reaction Steps
Into 50 mL of glacial acetic acid, 3.7 g of 1-methoxy-5-phenoxynaphthalene prepared as above, followed by 20 mL of 40% aqueous hydrogen bromide was stirred. The mixture was heated at 95-100° C. for 16 hours. The solvent was removed under vacuum, and the residue was redissolved in ethyl acetate and washed three times with brine. The organic layer was dried over magnesium sulfate and filtered. After removing solvent, the residue was chromatographed over silica gel with a gradient elution of 0 to 30% ethyl acetate in hexane, providing 2.10 g (59%) of 1-hydroxy-5-phenoxynaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090850 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-d1b49b4548f74fc59f1de55bc3c97665 |
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| Source note | uspto-grants-2000_07 |
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