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 p-anisoyl chloride as described in the procedure of Example 1 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 | US03983245 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-58b2c3ecba1c48bba9ceb0143e427104 |
| Source note | uspto-grants-1976_09 |