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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate | HCID 70984175 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-((tert-butoxycarbonyl)amino)prop-2-enoate | HCID 10932500 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-10c7dff811de4509b262b6f7d92fa579 |
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| Source note | uspto-grants-2014_11 |
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