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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519654Generated: October 26, 2026

Methanol → N2-(t-butoxycarbonyl)-N,N2,O-trimethyl-3-oxoserinamide

https://huagongshe.com/reaction/1519654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 22230—
ReactantMonomethylamine methanolHCID 57454252—
ReactantDiethyl [(t-butoxycarbonyl)(methyl)amino]propanedioateHCID 86679244—
SolventEthyl AcetateHCID 8857—
ProductN2-(t-butoxycarbonyl)-N,N2,O-trimethyl-3-oxoserinamideHCID 8667924534%

Reaction Steps

A 40% methylamine-methanol solution (67 mL) was added to a methanol (2.1 L) solution of diethyl [(t-butoxycarbonyl)(methyl)amino]propanedioate (Intermediate 3-1, 0.21 kg), and the mixture was stirred for 19 hours at room temperature. Further, a 40% methylamine-methanol solution (23 mL) was added, and the mixture was stirred for 4 days at the same temperature. Then, ethyl acetate (0.30 L) was added, and citric acid monohydrate (81 g) was slowly added under ice cooling, followed by stirring the mixture for 30 minutes under ice cooling. The precipitated solid was filtered, and the solvent was distilled off under reduced pressure. The resulting residue was purified by OH type silica gel column chromatography (gradient elution with hexane/ethyl acetate=75/25→15/85) to obtain N2-(t-butoxycarbonyl)-N,N2,O-trimethyl-3-oxoserinamide (Intermediate 4-2, yellow oil) (63 g, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-c2cc7ed1c3a446d7bd1598c997920759
Source noteuspto-grants-2015_07