HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367027Generated: October 31, 2026
Hydrochloric Acid → HCID 54356706, compound
https://huagongshe.com/reaction/367027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12751739 | HCID 12751739 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Product | HCID 54356706 | HCID 54356706 | — |
Reaction Steps
6 Grams of 5-hydroxy-3,4-dihydro-8-allyloxy-2(1H)-quinolinone was dissolved in 20 ml of dihydropyran, to this solution was added 2 ml of concentrated hydrochloric acid, then refluxed by heating for 1 hour. To this reaction mixture was added 5 g of potassium carbonate powder and stirred, then concentrated under reduced pressure. The residue thus obtained was extracted with ethyl acetate, the extract was washed with water, dried over anhydrous magnesium sulfate, again concentrated under reduced pressure to obtained pale yellow oily product. A mixed solvent of ethyl acetate-n-hexane was added to the oily product and allowed to stand for crystallization. There was obtained 8 g of 5-tetrahydropyranyloxy-8-allyloxy-3,4-dihydro-2(1H)-quinolinone as white amorphous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06133264 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-c20e5e6644794350a165cde4382be833 |
|---|
| Source note | uspto-grants-2000_10 |
|---|