HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11988Generated: October 25, 2026
6-Bromo-2-naphthalenol → 6-Bromo-1-chloronaphthalen-2-ol
https://huagongshe.com/reaction/11988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Catalyst | Zirconium chloride (ZrCl4), (T-4)- | HCID 9856075 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-1-chloronaphthalen-2-ol | HCID 22048159 | 95.4% |
Reaction Steps
The synthesis of (S1-2) was carried out following the method described in Synlett, No. 18, 2837 (2005), wherein 29.9 g of N-chlorosuccinimide and 600 ml of dichloromethane were added to a reactor in nitrogen atmosphere and cooled to 0° C., 2.6 g of zirconium (IV) chloride was added, and then 50 g of 6-bromo-2-naphthol (S1-1) was added slowly. The reaction solution was heated to room temperature and stirred for 10 hours, then washed with saturated sodium bicarbonate solution and water, dried over magnesium sulfate, and distilled under a reduced pressure to remove the solvent. Recrystallization was carried out using a mixed solvent of toluene/heptane=1/1 (volumetric ratio) to obtain 55 g of 6-bromo-1-chloro-2-naphthol (S1-2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727417B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-8195caeae8504cdfb40a16fc4ca39ca5 |
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| Source note | uspto-grants-2010_06 |
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