HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13066689, compound → HCID 13066714, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13066689 | HCID 13066689 | — |
| Reactant | HCID 20513503 | HCID 20513503 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Hydrogen iodide | HCID 24841 | — |
| Product | HCID 13066714 | HCID 13066714 | 51.6% |
Reaction Steps
A solution of 2-(2-methoxy-3-phenoxyphenyl)acetic acid (2.1 g) in acetic anhydride (10 ml) and hydriodic acid (55-58%, 20 ml) were treated in a similar manner to that of Example 10-(7). To the resultant oily residue containing 2-(2-hydroxy-3-phenoxyphenyl)acetic acid was added acetic anhydride (5 ml), and the mixture was refluxed under heating for 30 minutes and then evaporated. The oily residue (1.5 g) was purified by column chromatography (silica gel, benzene) and crystallization from ethanol to give 7-phenoxy-2,3-dihydrobenzofuran-2-one (950 mg). mp 60°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367238 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-97db403bd6334e0da91beeaae9e1b7e5 |
| Source note | uspto-grants-1983_01 |