HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 6-chloro-2-methyl-3(2H)-benzofuranone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-chloro-2-(1-(methoxycarbonyl)ethoxy)benzoate | HCID 19384699 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-2-methyl-3(2H)-benzofuranone | HCID 19384688 | 38.7% |
Reaction Steps
A solution of ethyl 4-chloro-2-(1-(methoxycarbonyl)ethoxy)benzoate (7.3 g) and 60% oil dispersion (1.5 g) of sodium hydride in tetrahydrofuran (70 ml) was heated at reflux for 30 minutes, and slowly cooled to room temperature. The reaction mixture was poured into ice-aqueous ammonium chloride and extracted with ether. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was subjected to chromatography on silica gel to give 6-chloro-2-methyl-3(2H)-benzofuranone (yield, 1.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05451607 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-002630c4d8a744178ec7dd85c9f1a245 |
| Source note | uspto-grants-1995_09 |