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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975462Generated: November 1, 2026

Dimethyl Sulfoxide → 1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-one

https://huagongshe.com/reaction/1975462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-olHCID 19099302—
SolventDichloromethaneHCID 6344—
Product1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-oneHCID 1909934777.5%

Reaction Steps

To a solution of 0.32 ml of oxalyl chloride in 10 ml of dichloromethane was added 0.54 ml of dimethyl sulfoxide at -78° C. under nitrogen. After stirring for 5 minutes, a solution of 1.00 g of 1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-ol in 2 ml of dichloromethane was added. After stirring for 30 minutes, 2.43 ml of triethylamine was added to the mixture and then the temperature of the mixture was raised to room temperature. The mixture was extracted with chloroform and the organic layer was washed in turn with 1N hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and brine, and dried over anhydrous magnesium sulfate. Evaporation of the solvent followed by a column chromatography on silica gel (hexane:ethyl acetate=1:1) gave 0.77 g of 1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286721
Source datasetuspto-grants-1994_02
ORD IDord-fa1df7b4e8754b6ea09f68dcf7018214
Source noteuspto-grants-1994_02