HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 20610270, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 20610271 | HCID 20610271 | — |
| Reactant | HCID 20610321 | HCID 20610321 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20610270 | HCID 20610270 | 83% |
Reaction Steps
A dimethyl formamide (260 mL) solution of 2-(5-Bromomethyl-isoxazol-3-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester (7.29 g, 56 mmol) and 2-allyloxycarbonylamino-malonic acid diethyl ester (8.25 g, 32 mmol) was cooled to 0° C. and cesium carbonate (25.41 g, 78 mmol) was added. The reaction was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was then poured into diethyl ether (2 L) and washed with water (5×200 mL) and brine. The organic portion was dried over magnesium sulfate and concentrated in vacuo. The crude residue was chromatographed on silica gel eluting with ethyl acetate:hexane (3:7) to afford the title compound as a clear colorless oil (10.95 g; 83%). MS (Cl) m/z 260.1 (M-99).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667331B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-8c18de4330464b78ac884cb782ed8bb1 |
| Source note | uspto-grants-2003_12 |