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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357935Generated: November 1, 2026

Dimethyl Sulfoxide → 1-Benzoylpiperidine-4-carbaldehyde

https://huagongshe.com/reaction/1357935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Piperidinemethanol, 1-benzoyl-HCID 10262870—
SolventDichloromethaneHCID 6344—
Product1-Benzoylpiperidine-4-carbaldehydeHCID 156812840.1%

Reaction Steps

To 1.99 g of dimethyl sulfoxide in 45 mL methylene chloride at −78° C. was added 2.16 g of oxalyl chloride. After 10 min, 1865 g of 4-hydroxymethyl-N-benzoylpiperidine (Step B) in 15 mL of methylene chloride was added at −78° C. and stirred for 30 min. DIEA (5.49 mL) was added and this mixture was stirred for an additional 30 min. at −78° C. and then warmed to room temperature and stirred another 30 min. The reaction was quenched with 50 mL water and extracted with 3×50 mL methylene chloride. The combined organic layers were dried over magnesium sulfate and evaporated under reduced pressure. The residue was chromatographed with 2:1 hexane:ethyl acetate followed by 1:1 hexane:ethyl acetate to give 1.445 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593346B2
Source datasetuspto-grants-2003_07
ORD IDord-367d0f872908449391ad8e187e1e5469
Source noteuspto-grants-2003_07