HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ethyl 2-(4-methoxyanilino)-4-oxofuran-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| Solvent | Diethylether ethylacetate | HCID 21584169 | — |
| Product | ethyl 2-(4-methoxyanilino)-4-oxofuran-3-carboxylate | HCID 2822533 | — |
Reaction Steps
Under a nitrogen atmosphere, to a mixed solution of ethyl 4-chloroacetoacetate (0.82 mL, 6.0 mmol) and 4-methoxyphenyl isocyanate 1.1 g, 7.2 mmol) in diethyl ether/ethyl acetate (10 mL/1.0 mL) that cooled with ice bath, triethylamine (0.96 mL, 6.9 mmol) was added dropwise. The reaction mixture was stirred at ambient temperature for 1.5 h then the precipitate was collected by filtration, washed with diethyl ether, 1M hydrochloric acid solution, water and diethyl ether, and then dried to afford ethyl 2-[(4-methoxyphenyl)amino]-4-oxo-4,5-dihydrofuran-3-carboxylate as solid (1.3 g, y. 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742113B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-027e28158d4e4b4d9793f0b3b60dd5a4 |
| Source note | uspto-grants-2014_06 |