HuagongsheHuagongshe Chemistry Print Report · For research reference only
2(3H)-Benzoxazolone → Ethyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2(3H)-Benzoxazolone | HCID 6043 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (2-oxo-1,3-benzoxazol-3(2H)-yl)acetate | HCID 590460 | 103.1% |
Reaction Steps
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]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432258B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-6f9c4ab4879644dc9c95565cbb051b37 |
| Source note | uspto-grants-2008_10 |