HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113660Generated: October 27, 2026
Water → 2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenone
https://huagongshe.com/reaction/2113660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Quinone | HCID 4650 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone | HCID 58604046 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenone | HCID 58604066 | — |
Reaction Steps
A solution of 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone (931 mg, 3.4 mmol) in acetonitrile (10 mL) was treated with benzoquinone (553 mg, 5.12 mmol), palladium(II) acetate (155 mg, 0.69 mmol), water (0.50 mL, 28 mmol), and perchloric acid (70%, ˜0.14 mL, 1.6 mmol). The resulting mixture was stirred overnight at room temperature. The mixture was partitioned between CH2Cl2 (200 mL) and water (100 mL) and the aqueous phase was back-extracted with CH2Cl2 (2×75 mL). The combined organics were washed with brine, dried over MgSO4, filtered, and concentrated under vacuum. The residue (1.17 g) was purified by Biotage™ (Charlottesville, Va.) flash chromatography on a 40S (4×7 cm) silica gel column, eluting with 10:1 to 5:1 hexane-EtOAc. The product-containing fractions were evaporated under vacuum to afford 2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432284B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-787cfc2492bd47d0ae9c3bf3d14a5fd4 |
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| Source note | uspto-grants-2008_10 |
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