HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-Chloro-2-(2-oxo-1,3-oxazolidin-3-yl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chloro-2-fluorobenzonitrile | HCID 93653 | — |
| Reactant | 2H-1,3-oxazol-2-id-4-one | HCID 53249566 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5-Chloro-2-(2-oxo-1,3-oxazolidin-3-yl)benzonitrile | HCID 66896096 | — |
Reaction Steps
(Step 1) To a solution (of 2-oxazolidone (1.23 g) in N,N-dimethylformamide (20 ml) was added sodium hydride (0.62 g) under ice-cooling, and the mixture was stirred for 5 min. 5-Chloro-2-fluorobenzonitrile (2.0 g) was added, and the mixture was stirred at room temperature for 2 hr. Saturated brine was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and filtered. The solvent was evaporated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to give 5-chloro-2-(2-oxo-1,3-oxazolidin-3-yl)benzonitrile (1.8 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07982044B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-37cec8130bfc4cb79db17d94661bfd42 |
| Source note | uspto-grants-2011_07 |