Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Ammonium fluoride | HCID 25516 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate | HCID 11098384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19036909 | HCID 19036909 | 113.9% |
Reaction Steps
3,4-Dihydro-6-trifluoromethylsulfonyloxy-1(2H)-naphthalenone (5.30 g, 18.0 mmol) was dissolved in 50 ml of N,N-dimethylformamide in an argon atmosphere, and 8.69 g (23.4 mmol) of 1-cyclohexenyltributyltin, 2.28 g (54.0 mmol) of lithium chloride and 0.63 g (0.90 mmol) of bistriphenylphosphinepalladium chloride were added to the solution. The mixture was stirred at 120° C. for 4 hours. The reaction product was cooled to room temperature, and ethyl acetate and a 2M-ammonium fluoride aqueous solution were added thereto, followed by stirring the mixture at room temperature overnight. The precipitate was filtered through Celite, and the filtrate was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was purified by silica-gel column chromatography (eluent: a mixture of 2% ethyl acetate and hexane) to obtain 2.32 g of the above-mentioned compound (yield 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646283 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-60b05b0a17534295950563e6d18a76cb |
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| Source note | uspto-grants-1997_07 |
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