HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871059Generated: October 31, 2026
3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenone → MLS003115617
https://huagongshe.com/reaction/871059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenone | HCID 266816 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | MLS003115617 | HCID 324518 | — |
Reaction Steps
A mixture of 500 mg. (2.4 mmol) 6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one was dissolved in anhydrous ethanol (10 ml) and Chloroform (10 ml). To this solution was added pyridinium tribromide (0.768 g, 2.4 mmol). The reddish brown mixture was heated with stirring at 50° C. for 20 min. The reaction mixture was then cooled and the solvent was evaporated. Then water (20 ml) was added to the residue and it was then extracted with 50 ml of dichloromethane. The dichloromethane layer was then washed with 10% sodium bicarbonate solution (50 ml) followed by water (50 ml). The organic layer was then dried and the solvent was evaporated in vacuum to yield the crude product, 2-bromo-6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one which was purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969573B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-991c20f6500d46e8a413b273bf45fe46 |
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| Source note | uspto-grants-2015_03 |
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