HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 59135088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86603418 | HCID 86603418 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59135088 | HCID 59135088 | — |
Reaction Steps
To a solution of [(1S,2S)-2-(3,5-difluorophenyl)-2-hydroxy-1-methylethyl]carbamate (900 mg, 2.80 mmol) in THF (28.6 mL) was added MeOH (14.3 mL) and 7.5 N KOH (7.2 mL). The reaction was stirred at room temperature for 4 hours and then extracted with EtOAc (2×75 mL). The organic extracts were washed with water and brine (50 mL each), dried over Na2SO4, filtered, and concentrated. Purification of the residue by flash chromatography on silica gel (10 to 75% EtOAc/hexanes) afforded (4S,5S)-5-(3,5-difluorophenyl)-4-methyl-1,3-oxazolidin-2-one. Rf=0.07 (25% EtOAc/hexanes). LCMS=214.3 (M+1)+. 1H NMR (CDCl3, 500 MHz) δ 6.89-6.93 (m, 2H), 6.82 (m, 1H), 6.24 (bs, 1H), 5.01 (d, J=6.8 Hz, 1H), 3.79 (m, 1H), 1.42 (d, J=6.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735435B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-e353195f0b7d4f8181c14e993060e5b7 |
| Source note | uspto-grants-2014_05 |