HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → (4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-4-(2-Hydroxy-2-methylpropyl)oxazolidin-2-one | HCID 11321109 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone | HCID 11194496 | — |
Reaction Steps
A dichloromethane solution (100 mL) of the alcohol (47.8 g) from Step 3 was added to a −70° C. solution of (diethylamino)sulfur trifluoride (48.5 g) in dichloromethane (500 mL). The mixture was warmed to room temperature and stirred for 1 hour. The mixture was then carefully added to a 0° C. mixture of saturated aqueous NaHCO3 (800 mL). The organic layer was separated and washed with saturated aqueous NaHCO3. The aqueous was further extracted with dichloromethane (100 mL) and the combined dichloromethane layers were dried and concentrated. The residue was purified by chromatography on SiO2 using ethyl acetate and hexanes (1:5) followed by ethyl acetate to yield (4S)-4-(2-fluoro-2-methylpropyl)-1,3-oxazolidin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973037B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-0410e3be895b4d60a2a2bd3bcc688941 |
| Source note | uspto-grants-2011_07 |