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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49443Generated: October 25, 2026

Dimethyl Sulfoxide → 1-(4-Methylbenzyl)piperidin-4-one

https://huagongshe.com/reaction/49443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(4-Methylbenzyl)piperidin-4-olHCID 791482—
SolventDichloromethaneHCID 6344—
Product1-(4-Methylbenzyl)piperidin-4-oneHCID 1195954181%

Reaction Steps

To 2.8 mL (32 mmol) of oxalyl chloride in 75 mL of CH2Cl2 at −78° C. was added 4.6 mL (64 mmol) of DMSO. To this mixture was added 5.3 g (26 mmol) of 1-(4-methylbenzyl)-4-piperidinol 123 in 10 mL of CH2Cl2, and the mixture was stirred 5 min in the cold. The mixture was quenched with 18 mL (129 mmol) of triethylamine and allowed to come to room temperature, and saturated aqueous ammonium chloride was added. The organic phase was washed with water and brine, dried, and evaporated to give 4.27 g (81%) of 1-(4-methylbenzyl)-4-piperidinone (124), which was used as is without further purification. GC/MS showed 100% purity with a molecular ion of 203.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706740B2
Source datasetuspto-grants-2004_03
ORD IDord-fb7270a74cbc4031b8e83c2f70138da2
Source noteuspto-grants-2004_03