HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367030Generated: October 30, 2026
Potassium Carbonate → HCID 12861683, compound
https://huagongshe.com/reaction/367030
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12751880 | HCID 12751880 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12861683 | HCID 12861683 | — |
Reaction Steps
9.16 Grams of 5-acetoxy-8-tetrahydropyranyloxy-3,4-dihydro-2(1H)-quinolinone was dissolved in 200 ml of methanol, to this solution was added 45 ml of an aqueous solution of 10%-potassium carbonate, refluxed by heating for 1 hour, then concentrated to dryness under reduced pressure, there was obtained 5-hydroxy-8-tetrahydropyranyloxy-3,4-dihydro-2(1H)-quinolinone. This product was suspended in 100 ml of DMF, further 4.1 g of potassium carbonate was added to this suspension and stirred. To this mixture was added 3 ml of allyl bromide at room temperature and stirred for 8 hours. To this reaction mixture was added 200 ml of water, and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane, there was obtained 6 g of 8-tetrahydropyranyloxy-5-allyloxy-3,4-dihydro-2(1H)-quinolinone as white solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133264 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-d92495e51f9c4cbf92e3e8dc6748481c |
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| Source note | uspto-grants-2000_10 |
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