HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Carbamate → Ethyl 2-(methoxycarbonylamino)-3-methylbut-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Carbamate | HCID 11722 | — |
| Reactant | Ethyl 3-methyl-2-oxobutyrate | HCID 88406 | — |
| Reactant | Pyridine 4-methylbenzene-1-sulfonate | HCID 161440 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 2-(methoxycarbonylamino)-3-methylbut-2-enoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921514B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-1f4fbea6feaf4fb0988e35d1703a06ce |
| Source note | uspto-grants-2014_12 |