HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyl iodide → 7-fluoro4-isobutyl-2H-1,4-benzoxazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 13731295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-fluoro4-isobutyl-2H-1,4-benzoxazin-3(4H)-one | HCID 19047164 | 65% |
Reaction Steps
To 3.96 g (99 mmol) of hexanes washed 60% sodium hydride in 150 ml of N,N-dimethylformamide was added portionwise as a solid 15 g (90 mmol) of 7-fluoro-2H-1,4-benzoxazin-3(4H)-one. When the addition was complete the reaction was stirred at room temperature for 10 min, after which time 19.8 g (108 mmol) of isobutyl iodide was added. The reaction was then stirred overnight before quenching onto 200 ml of water. The aqueous phase was extracted with EtOAc (2×150 ml) and the combined organics were dried over Na2SO4, filtered and evaporated in vacuo to give the desired alkylated product, as a yellow oil (13 g, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05238908 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-96fa3999b9b647e2923fb0aa70ddfb65 |
| Source note | uspto-grants-1993_08 |