HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383042Generated: October 30, 2026
Potassium Fluoride → HCID 59396515, compound
https://huagongshe.com/reaction/2383042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 67538221 | HCID 67538221 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59396515 | HCID 59396515 | 63.9% |
Reaction Steps
7-bromo-1-cyclohexyl-3,4-dihydroisoquinoline (4.01 g) was dissolved in 1,4-dioxane (100 mL), to which tributyl(1-ethoxyvinyl)tin (7.43 g), potassium fluoride (2.39 g), and tetrakis(triphenylphosphine)palladium (1.58 g) were then added, followed by stirring at 80° C. for 5 hours. Thereafter, to the reaction liquid were further added tributyl(1-ethoxyvinyl)tin (2.47 g) and tetrakis(triphenylphosphine)palladium (1.58 g), followed by stirring for 14 hours. Then, the reaction liquid was filtered through celite and the insoluble materials were separated. 4 M HCl/dioxane (20 mL) was added to the insoluble materials, followed by stirring at 60° C. for 30 minutes. The solvent was evaporated and water was added to the mixture which was then extracted with EtOAc. The extract was washed with saturated brine, and then dried over magnesium sulfate. The solvent was evaporated and the resulting residue was purified by silica gel column chromatography (chloroform-MeOH) to obtain 1-(1-cyclohexyl-3,4-dihydroisoquinolin-7-yl)ethanone (2.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263607B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-32b86e758cb64827adf12c1e9d297da5 |
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| Source note | uspto-grants-2012_09 |
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