HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840872Generated: October 30, 2026
Hydrochloric Acid → 6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1840872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | 6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 10729589 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 23444702 | 67% |
Reaction Steps
A solution of 6-bromo-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (Intermediate 4, 270 mg, 1.06 mmol) in 5 ml of THF was first degassed by bubbling with argon for 30 min. Tributyl(1-ethoxyvinyl)tin (766 mg, 2.12 mmol) and PdCl2(PPh3)2 (37mg, 0.05 mmol) were added. After stirring at 80° C. for 18 h, the mixture was cooled to room temperature and 3 mL of 10% HCl was added. The mixture was then stirred for another 30 min before extracted with ethyl acetate (3×10 mL). The combined organic layer was washed with brine (1×10 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chormatography (50:50 hexane/ethyl acetate) yielded the title compound as a white solid (154 mg, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683092B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-2284227a08b34a7f97e9de14f83ae5b1 |
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| Source note | uspto-grants-2004_01 |
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