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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037734Generated: November 2, 2026

tert-Butyl (2-(methoxy(methyl)amino)-2-oxoethyl)carbamate → tert-butyl N-(2-oxopropyl)carbamate

https://huagongshe.com/reaction/2037734

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2-(methoxy(methyl)amino)-2-oxoethyl)carbamateHCID 4428209—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-(2-oxopropyl)carbamateHCID 35795572%

Reaction Steps

To a solution of tert-butyl 2-(methoxy(methyl)amino)-2-oxoethylcarbamate (4.36 g, 0.02 mol) in THF (50 mL) added MeMgBr (40 ml, 0.08 ol) at −78° C. The formed mixture was stirred overnight. The mixture was quenched with NH4Cl and extracted with EtOAc. The organic phase was separated, dried over anhydrous Na2SO4, concentrated and purified by column chromatography to give tert-butyl 2-oxopropylcarbamate (2.5 g, 72%). 1H NMR (400 MHz, CDCl3): δ=1.42 (s, 9H), 2.18 (s, 3H), 4.01 (s, 2H), 5.22 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-ee14afc0a8d647029fc37246ce71ef5f
Source noteuspto-grants-2013_11