HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3(2H)-Benzofuranone, 6-(phenylmethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Hydroxy-3-coumaranone | HCID 235717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3(2H)-Benzofuranone, 6-(phenylmethoxy)- | HCID 10633774 | 95.9% |
Reaction Steps
To a stirred solution of 6-hydroxy-3-oxo-2,3-dihydrobenzofuran of Example 10(a) (32 kg, 213 moles) in DMF (192 L) was added potassium carbonate (31.0 kg, 224 moles). After stirring for 5 min. at room temperature, benzyl bromide (45.2 kg, 264 moles) was added and the resulting mixture was stirred for 2 hours at room temperature. The mixture was poured into water (651 L), stirred for 30 minutes and the product collected by centrifugation. The crude solid was washed with water (580 L), 80% ethanol (100 L) and dried under vacuum to afford the desired product (49.1 kg, 95%) which was used without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663368 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-0e9ef87909fa42cb82849705683db1c1 |
| Source note | uspto-grants-1997_09 |