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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264773Generated: October 31, 2026

Chloride → HCID 19036909, compound

https://huagongshe.com/reaction/264773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantAmmonium fluorideHCID 25516—
ReactantLithium ChlorideHCID 433294—
Reactant5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonateHCID 11098384—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 19036909HCID 19036909113.9%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646283
Source datasetuspto-grants-1997_07
ORD IDord-60b05b0a17534295950563e6d18a76cb
Source noteuspto-grants-1997_07