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 | 2-(4-Chlorophenyl)-3-(4-methoxybenzoyl)benzofuran | HCID 21435260 | — |
| Product | 2-(4-Chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran | HCID 21435269 | — |
Reaction Steps
Acylation of 2-(4-chlorophenyl)benzofuran with p-anisoyl chloride followed by demethylation of the 2-(4-chlorophenyl)-3-(4-methoxybenzoyl)benzofuran thus formed by procedures described above gives 2-(4-chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947470 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-574e68acb873454380dbadfee793eb74 |
| Source note | uspto-grants-1976_03 |