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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643471Generated: October 31, 2026

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

https://huagongshe.com/reaction/1643471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperidin-2-ylmethanolHCID 94263—
Reactant4-Methoxy-2,6-dimethylbenzene-1-sulfonyl chlorideHCID 15917496—
Product[1-(4-Methoxy-2,6-dimethyl-phenylsulfonyl)-piperidin-2-yl]-methanolHCID 43574491—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of triethylamine (2.5 eq) and 4-methoxy-2,6-dimethylbenzenesulfonyl chloride (13.04 mmol, 1 eq) in MC (10 ml) was added dropwise to a solution of piperidin-2-ylmethanol (13.04 mmol) in MC (30 ml) at 0° C. and the mixture was stirred at 0° C. for 30 min. It was then stirred at room temperature for 14 h, MC (50 ml) was subsequently added to the mixture and the mixture was washed with water and sat. sodium chloride solution. The organic phase was dried (Na2SO4) and concentrated in vacuo. The crude product obtained in this way was purified by column chromatography. Yield: 3.2 g (79%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-08474fc324b94ea095e7c9a0872e0716
Source noteuspto-grants-2012_02