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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624283Generated: October 26, 2026

Dimethyl Sulfoxide → tert-Butyl 3-(2-oxoethyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/624283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl 3-(2-hydroxyethyl)azetidine-1-carboxylateHCID 22594530—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-(2-oxoethyl)azetidine-1-carboxylateHCID 53415272—

Reaction Steps

To a solution of oxalyl chloride (488 μl, 5.58 mmol) in 40 ml dichloromethane at −78° C. was added dimethyl sulfoxide (792 μl, 11.16 mmol) dropwise by syringe. The mixture was stirred for 15 minutes at −78° C. when a solution of tert-butyl 3-(2-hydroxyethyl)azetidine-1-carboxylate (936 mg, 4.65 mmol) in 10 ml dichloromethane was added dropwise by syringe. After 1 hour at −78° C., triethylamine (3241 μl, 23.25 mmol) was added and the suspension was warmed to room temperature and stirred for an additional hour. The mixture was quenched with water (25 ml) and saturated aqueous potassium carbonate (10 ml), stirred vigorously and separated. The aqueous layer was extracted with dichloromethane (2×20 ml) and the combined organic layers were dried with magnesium sulfate, filtered and concentrated. The crude material was flash chromatographed to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-9252ec245fb54af1924baf08d272b632
Source noteuspto-grants-2016_04