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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243303Generated: November 2, 2026

Dimethyl Sulfoxide → Tert-butyl 3-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1243303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825103%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of DMSO (7.8 mL, 109.3 mmol) and methylene chloride (100 mL) was cooled to −78° C. Oxalyl chloride (4.8 mL, 54.7 mmol) was added to this solution via syringe. The mixture was stirred at −78° C. for 30 min. A solution of 3-hydroxypiperidine-1-carboxylic acid tert-butyl ester (10.0 g, 49.7 mmol) in methylene chloride (30 mL) was added dropwise to this solution (temperature remained below −70° C.). The mixture was stirred for 30 min. Triethylamine (28 mL, 200 mmol) was added dropwise over 20 min. The mixture was stirred at −78° C. for 1 h and was allowed to warm to room temperature and stirred for 45 min. The mixture was diluted with water, and the layers separated. The organic layer was washed with water, dried (Na2SO4), filtered, and concentrated to give 3-oxopiperidine-1-carboxylic acid tert-butyl ester (10.2 g) as a yellow, brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119089B2
Source datasetuspto-grants-2006_10
ORD IDord-d30f3e2e755947d6b771fea6ac41c94c
Source noteuspto-grants-2006_10