HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51631Generated: October 29, 2026
6-Methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one → 6-hydroxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one
https://huagongshe.com/reaction/51631
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 12415147 | — |
| Solvent | Boron tribromide | HCID 25134 | — |
| Product | 6-hydroxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 13412253 | 52.6% |
Reaction Steps
A stirred, cooled (−78° C.) solution of 6-methoxy-4,4-dimethyl-1,2,3,4-tetrahydronaphthalene-1-one (Intermediate 9, 0.8, 3 mmol) under argon was treated with a 1M solution of boron tribromide (10 mL). The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was cooled to −78° C., quenched and diluted with saturated aqueous sodium bicarbonate solution and the aqueous phase was extracted with dichloromethane (×2). The combined organic phase was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to an oil. Flash column chromatography over silica gel (230-400 mesh) using 30% ethyl acetate in hexane as the eluent afforded the title compound (0.3 g, 52%) as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713647B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-a4dd4af1e0e44ce284bab7c6b17d2b50 |
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| Source note | uspto-grants-2004_03 |
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