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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339015Generated: October 25, 2026

Potassium Carbonate → Methyl 2-((tert-butoxycarbonyl)amino)prop-2-enoate

https://huagongshe.com/reaction/339015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoateHCID 70984175—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((tert-butoxycarbonyl)amino)prop-2-enoateHCID 1093250081%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate (36.0 g, 102 mmol), K2CO3 (28.2 g, 204 mmol) and DMF (204 mL) was heated at 65° C. for 1 hour. After cooling, the reaction mixture was partitioned between ether and water. The aqueous layer was extracted with ether. The combined organic layers were washed with water and brine, dried and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (10:1 hexanes/EtOAc) to give methyl 2-(tert-butoxycarbonylamino)acrylate (16.5 g, 81%) as a colorless oil, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-10c7dff811de4509b262b6f7d92fa579
Source noteuspto-grants-2014_11