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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411396Generated: October 25, 2026

Methyl Carbamate → Ethyl 2-(methoxycarbonylamino)-3-methylbut-2-enoate

https://huagongshe.com/reaction/1411396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl CarbamateHCID 11722—
ReactantEthyl 3-methyl-2-oxobutyrateHCID 88406—
ReactantPyridine 4-methylbenzene-1-sulfonateHCID 161440—
SolventBenzeneHCID 241—
ProductEthyl 2-(methoxycarbonylamino)-3-methylbut-2-enoateHCID 11117085—

Reaction Steps

A benzene solution (90 mL) of ethyl-3-methyl-2-oxobutanoate (4.03 g, 28.0 mmol), methyl carbamate (2.098 g, 28.0 mmol) and pyridine 4-methylbenzenesulfonate (0.70 g, 2.80 mmol) was heated to reflux in a round bottom flask equipped with a Dean-Stark trap and reflux condenser. After 44 hours of heating the mixture was cooled and then partitioned between ethyl acetate (50 mL) and brine (50 mL). The organic phase was washed with brine (2×50 mL) then dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography on silica gel (ethyl acetate-hexanes) to provide the title compound as an off white crystalline solid (1.487 g, 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921514B2
Source datasetuspto-grants-2014_12
ORD IDord-1f4fbea6feaf4fb0988e35d1703a06ce
Source noteuspto-grants-2014_12