HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7819Generated: October 23, 2026
Methyl vinyl ketone → 5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone
https://huagongshe.com/en/reaction/7819
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-Methoxy-2-methylindan-1-one | HCID 12290490 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone | HCID 21990908 | 332.6% |
Reaction Steps
A solution of 5-methoxy-2-methyl-1-indanone (0.5 g, 2.84 mmol) in anhydrous tetrahydrofuran (3 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (0.085 mL, 0.57 mmol) and methyl vinyl ketone (0.473 mL, 5.68 mmol). The resulting solution was placed under a nitrogen atmosphere and stirred at room temperature overnight. The mixture was diluted with EtOAc (25 mL), washed with 0.2N HCl (25 mL) and brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to a yellow oil (800 mg). The oil was dissolved in CH2Cl2 (10 mL) and the solution added to a small column of EM silica gel 60 (8 mL). The column was eluted with CH2Cl2 (30 ml) and the eluant evaporated under vacuum to afford 5-methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone (467 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087599B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-b2f702acf9204650b931ca10badf77fa |
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| Source note | uspto-grants-2006_08 |
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