HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → 2-(4-Chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | 2-(4-Chlorophenyl)-1-benzofuran | HCID 4368312 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 2-(4-Chlorophenyl)-3-(4-methoxybenzoyl)benzofuran | HCID 21435260 | — |
| Product | 2-(4-Chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran | HCID 21435269 | — |
Reaction Steps
When 2-(4'-chlorophenyl)benzofuran was acylated with anisoyl chloride was described in the procedure of Example 10 and the resulting 2-(4'-chlorophenyl)-3-(4'-methoxybenzoyl)benzofuran was demethylated with pyridine hydrochloride as previously described, 2-(4'-chlorophenyl)-3-(4'-hydroxybenzoyl)benzofuran was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975537 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-bb0180e88aad4302bb8aea0542a7b9d2 |
| Source note | uspto-grants-1976_08 |