HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid ethyl ester | HCID 57875802 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid | HCID 57875816 | 90.9% |
Reaction Steps
NaOH (34 mg, 8.5 mmol) was added to a solution of N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid ethyl ester (292 mg, 1.0 mmol) in the mixture of THF (13 mL) and H2O (13 mL) and stirred for 1 hr at room temperature. The reaction mixture was concentrated and the obtained residue was diluted with water, acidified with concentrated HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over Na2SO4 and concentrated to afford 40 mg (90.9% Yield) of N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039463B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-bfdb5dd771a44f1695541b673278d3d2 |
| Source note | uspto-grants-2011_10 |