HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Benzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-(4-Fluorophenyl)oxazolidine-2,5-dione | HCID 86649049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylate | HCID 11438888 | 64.1% |
Reaction Steps
To a solution of 4-(4-fluorophenyl)oxazolidine-2,5-dione (2.5 g, 12.8 mmol) in THF (30 mL) cooled to −25° C. was added benzyl chloroformate (2.3 mL, 16.6 mmol), followed by the slow addition (˜10 min) of N-methylmorpholine (2.11 mL, 19.2 mmol) as a solution in THF (5 mL). The solution was stirred at this temperature for 1 h. and then allowed to warm to rt overnight. The resulting solution was filtered through Celite, and the filtrate was concentrated. The resulting crude material was recrystallized from 2:2:1 t-butyl methyl ether:hexanes:THF to give benzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylate (2.7 g, 64%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09308207B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-0d89d39743bb41238d6a0d06399a9d11 |
| Source note | uspto-grants-2016_04 |