HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400314Generated: November 2, 2026
Hydrogen Bromide → 6-Bromo-1-chloronaphthalen-2-ol
https://huagongshe.com/reaction/1400314
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-Chloro-2-naphthol | HCID 12459 | — |
| Solvent | Hydrogen Peroxide | HCID 784 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-1-chloronaphthalen-2-ol | HCID 22048159 | — |
Reaction Steps
To a solution of 400 mg (2.24 mmol) of 1-chloronaphthalen-2-ol in 3 mL of MeOH, HBr (purum p.a., ≧62%, 270 μL) and H2O2 (50 wt. % in water solution, 27 μL) were added. The resulting mixture was heated at 40° C. and stirred overnight. The mixture was quenched with water (10 mL) and extracted with ethyl acetate (10 mL×2). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to afford 6-bromo-1-chloronaphthalen-2-ol as pale yellow solid which was used in the next step without further purification. HPLC-MS (ESI+): m/z 258.51 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906946B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9078dd4278fc4761b10edbc740a437f8 |
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| Source note | uspto-grants-2014_12 |
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