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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643460Generated: October 26, 2026

Triethylborane → Perfluorophenyl 3-(1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)propane-1-sulfonate

https://huagongshe.com/reaction/1643460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantPentafluorophenyl vinylsulfonateHCID 2763990—
Reactant2-(Iodomethyl)-1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidineHCID 59367752—
ReactantHCID 178462538HCID 178462538—
SolventDichloromethaneHCID 6344—
ProductPerfluorophenyl 3-(1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)propane-1-sulfonateHCID 59367793—

Reaction Steps

1-Ethylpiperidine hypophosphite (1.184 g, 6.614 mmol) were weighed into the reaction flask under an inert gas, and methylene chloride (10 ml) was added. The solution was cooled with ice-water, and 2,3,4,5,6-pentafluorophenyl 1-ethylenesulfonate (0.218 g, 0.794 mmol) [Org. Lett.; 2002; 4(15); 2549-2551] and 2-(iodomethyl)-1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidine (0.28 g, 0.661 mmol) was added at 0° C. Triethylborane solution (0.03 ml, 1 mol/l) was added to the reaction mixture and compressed air was then passed through the mixture for 10 sec. After stirring for 5 min the addition of triethylborane solution-compressed air was repeated with the same amount. After thin layer chromatography control, the addition of triethylborane soln.-compressed air was repeated again with the same amount. The reaction mixture was washed with cooled water (10 ml) and cooled saturated sodium bicarbonate soln. (10 ml), dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica gel) with hexane/diethyl ether/methylene chloride (6:1:1) Yield: 50 mg (13%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-9123c3927a3b457b922acaa2905f4b69
Source noteuspto-grants-2012_02