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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429820Generated: October 29, 2026

Dimethyl Sulfoxide → 1-(Methylsulfonyl)piperidine-4-carbaldehyde

https://huagongshe.com/reaction/429820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(1-(Methylsulfonyl)piperidin-4-yl)methanolHCID 18352755—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfonyl)piperidine-4-carbaldehydeHCID 1095437274.7%

Reaction Steps

A solution of dimethylsulfoxide (39 ml, 0.55 mole) in dichloromethane (300 ml) was added slowly to a solution of oxalyl chloride (22.7 ml, 0.264 mole) in dichloromethane (700 ml) at −60° C. After 10 minutes a solution of 1-methanesulfonylpiperidine-4-methanol (46 grams. 0.238 mole) in dichloromethane (500 ml) was added slowly. After 30 minutes at −60° C., triethylamine (167 ml) was added. The mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate (1.2 liters) and water (200 ml). The organic phase was dried (anhydrous magnesium sulfate) and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to give 1-methanesulfonylpiperidine-4-carboxaldehyde (34 grams), m.p. 97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319920B1
Source datasetuspto-grants-2001_11
ORD IDord-17a21b5be76149768f8a603b6672d50d
Source noteuspto-grants-2001_11