Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519657Generated: October 25, 2026

Potassium Hydroxide → N-(t-butoxycarbonyl)-O-ethyl-N-methyl-3-oxoserine

https://huagongshe.com/reaction/1519657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDiethyl [(t-butoxycarbonyl)(methyl)amino]propanedioateHCID 86679244—
SolventEthanolHCID 702—
ProductN-(t-butoxycarbonyl)-O-ethyl-N-methyl-3-oxoserineHCID 86679248—

Reaction Steps

An ethanol solution (4.0 mL) of potassium hydroxide (0.19 g) prepared under ice cooling was added to an ethanol (2.0 mL) solution of diethyl [(t-butoxycarbonyl)(methyl)amino]propanedioate (Intermediate 3-1, 1.0 g), and the mixture was stirred for 23 hours at room temperature. The reaction mixture was concentrated under reduced pressure, and a 1.0 mol/L-sodium hydrogen carbonate aqueous solution was added, followed by extracting the mixture with ethyl acetate. The aqueous layer was cooled with iced water, and potassium hydrogen sulfate was added to adjust it to pH 2, followed by extracting the mixture with chloroform. The extract was dried over anhydrous sodium sulfate, and the desiccant was filtered out. Then, the solvent was distilled off under reduced pressure to obtain N-(t-butoxycarbonyl)-O-ethyl-N-methyl-3-oxoserine (Intermediate 7-1, light yellow oil) (0.26 g, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-8e104b00e4ae4ebdae33260dd9063fbf
Source noteuspto-grants-2015_07