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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697086Generated: October 31, 2026

Piperidin-4-ol → 4-((4-Hydroxypiperidin-1-yl)sulfonyl)benzaldehyde

https://huagongshe.com/reaction/1697086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Formylbenzene-1-sulfonyl chlorideHCID 2759210—
SolventDichloromethaneHCID 6344—
Product4-((4-Hydroxypiperidin-1-yl)sulfonyl)benzaldehydeHCID 86624855—

Reaction Steps

To 4-formyl-benzenesulfonyl chloride (1.0 g) in DCM (10 mL) was added 4-hydroxypiperidine (0.984 g), followed by NaHCO3 (10 mL, aq sat'd) and the mixture stirred for 2 h at RT. The aqueous layer was washed with DCM (2×25 mL), and the combined organic portions washed with brine, dried over Na2SO4, filtered, and the solvent removed under reduced pressure to provide 4-(4-hydroxypiperidine-1-sulfonyl)benzaldehyde. The product was purified on anhydrous silica (10% MeOH/DCM). M+H 269.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163906B2
Source datasetuspto-grants-2012_04
ORD IDord-d4f28b959ab341d69b62e4980688dec1
Source noteuspto-grants-2012_04