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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171766Generated: November 3, 2026

Dimethyl Sulfoxide → 1-Boc-piperidine-3-carboxaldehyde

https://huagongshe.com/reaction/1171766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Boc-piperidine-3-carboxaldehydeHCID 996444893.8%

Reaction Conditions

Temperature-68 °C

Reaction Steps

DMSO (0.18 mL, 2.6 mmol) in CH2Cl2 (5 mL) was added dropwise to a solution of oxalyl chloride (2M in CH2Cl2, 0.65 mL, 1.3 mmol) in CH2Cl2 (4 mL) at −78° C. The resulting mixture was stirred at −68° C. for 15 minutes. 3-Hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (Dean A. Wacker et al. Bioorganic & Medicinal Chemistry Letters 2002, 12, 1785-1789) (0.22 g, 1.0 mmol) in CH2Cl2 (4 mL) was added dropwise and after 15 min stirring at −78° C., Et3N (6 mL) was added. The resulting solution was stirred at ambient temperature for 16 h. Water was added and the mixture was extracted with diethyl ether, the organic layer was dried (Na2SO4) and concentrated to give the product as an yellow oil (0.20 g, 92% yield). This crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829707B2
Source datasetuspto-grants-2010_11
ORD IDord-5c06e1106b2f4d9e820ad4fe73bdedfa
Source noteuspto-grants-2010_11