HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418808Generated: November 2, 2026
Bromine → 7-Bromo-3,4-dihydro-5,8-dimethyl-1(2H)-naphthalenone
https://huagongshe.com/reaction/1418808
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl- | HCID 99334 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-3,4-dihydro-5,8-dimethyl-1(2H)-naphthalenone | HCID 53761320 | 100% |
Reaction Steps
To a solution of 15.0 g of 5,8-dimethyltetralone (purchased from Wiley Organics) in 250 mL of methylene chloride was added 28.7 g of aluminum chloride (purchased from Aldrich Chemical Co.). The mixture was cooled to 0° C. and then a solution of 15.2 g bromine in 90 mL of methylene chloride was added dropwise. After the mixture was stirred at room temperature for 2 h, it was cooled to 0° C. and then approximately 200 g of ice was added. The resulting mixture was filtered. The organic layer was separated and was washed with 1N aqueous sodium hydroxide, dried over MgSO4, filtered, and concentrated under reduced pressure. The resulting solid was crystallized from 1-chlorobutane to give 21.8 g of the title compound of Step A as a solid melting at 64°-68° C. 1H NMR (CDCl3): δ 2.11 (m, 2H), 2.25 (s, 3H), 2.64 (t, 2H), 2.66 (s, 3H), 2.77 (t, 2H), 7.53 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885936 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-777d173851df4b528eeb888b17c361f4 |
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| Source note | uspto-grants-1999_03 |
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