HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2(3H)-Benzoxazolone → Ethyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2(3H)-Benzoxazolone | HCID 6043 | — |
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetate | HCID 590460 | 103,1% |
Reaktionsschritte
A solution of 1,3-benzoxazol-2(3H)-one (676 mg, 5.0 mmol) in (5 mL) was added to a suspension of NaH (220 mg, 5.5 mmol) in DMF (5 mL) at room temperature, and the resulting solution was stirred for 1 h. Ethyl bromoacetate (0.55 mL, 5.0 mmol) was added to the reaction mixture, and stirring was continued for 2 h. The reaction was quenched with water (10 mL) and extracted with EtOAc (2×20 mL). The organic extracts were combined and washed with water, brine, and dried (Na2SO4). The solvent was removed under reduced pressure to give the title compound (1.14 g, >100%) as a brown solid. MS (ES) m/e 222 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07749998B2 |
| Quelldatensatz | uspto-grants-2010_07 |
| ORD ID | ord-93090c895ceb407c8ebfea98132bc389 |
| Quellennotiz | uspto-grants-2010_07 |