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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643457Generated: October 25, 2026

Piperidin-2-ylmethanol → [1-(4-Methoxy-2,6-dimethyl-phenylsulfonyl)-piperidin-2-yl]-methanol

https://huagongshe.com/reaction/1643457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-2-ylmethanolHCID 94263—
ReactantPerfluorophenyl 4-methoxy-2,6-dimethylbenzenesulfonateHCID 59746536—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDimethylformamideHCID 6228—
Product[1-(4-Methoxy-2,6-dimethyl-phenylsulfonyl)-piperidin-2-yl]-methanolHCID 43574491—

Reaction Conditions

Temperature110 °C

Reaction Steps

Perfluorophenyl 4-methoxy-2,6-dimethylbenzenesulfonate (1 g, 2.616 mmol), 2-(hydroxymethyl)-piperidine (1.61 g, 13.079 mmol) and tetrabutylammonium chloride (1.45 g, 5.231 mmol) were dissolved in N,N-dimethylformamide (10 ml) and the solution was stirred at 110° C. for 1 h. The solvent was removed in vacuo, the residue was dissolved in ethyl acetate and the solution was washed with ammonium chloride solution (10%, 20 ml), dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica gel) with diethyl ether/hexane/methylene chloride (1:1:1). Yield: 0.63 g (76%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-f06854afd3cf4fe5846e8e0bf8757fd8
Source noteuspto-grants-2012_02