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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930111Generated: October 27, 2026

4-Methylmorpholine → Ethyl 2-(2-((tert-butoxycarbonyl)amino)propanamido)-3-oxobutanoate

https://huagongshe.com/reaction/1930111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-N-Boc-aminopropionic acidHCID 268471—
ReactantButanoic acid, 2-amino-3-oxo-, ethyl ester, 4-methylbenzenesulfonate (1:1)HCID 86636663—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-((tert-butoxycarbonyl)amino)propanamido)-3-oxobutanoateHCID 5799215968.7%

Reaction Conditions

Temperature-25 °C

Reaction Steps

A solution of 4-methylmorpholine (900 g) in THF (15 L) was added to 2-(tert-butoxycarbonylamino)propanoic acid (1690 g, 8933.17 mmol). The mixture was cooled to −25° C. and isobutyl chloroformate (1.164 L, 8933.17 mmol) was added. After 20 minutes the second equivalent of 4-methylmorpholine (900 g) was added followed by ethyl 2-amino-3-oxobutanoate Tosylate salt (see J-P. Genet et al, Eur. J. Org. Chem., 2004, 3017-3026) (2700 g, 8507.78 mmol) suspended in THF (2.5 L). The mixture was stirred at −25° C. for 30 minutes and then left to warm to ambient temperature overnight. The reaction was quenched with water (15 L), extracted with EtOAc (3×5 L) and the combined extracts washed with 50% saturated brine (5 L). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 50 to 80% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford ethyl 2-(2-(tert-butoxycarbonylamino)propanamido)-3-oxobutanoate (1850 g, 68.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-ec8584dd9c77493fbd3557fc79beef21
Source noteuspto-grants-2012_05