HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Chlorophenyl)-1-benzofuran → 2-(4-Chlorophenyl)-3-[4-(3-diethylaminopropoxy)benzoyl]benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Chlorophenyl)-1-benzofuran | HCID 4368312 | — |
| Reactant | 4-(3-Diethylaminopropoxy)benzoyl chloride hydrochloride | HCID 21435314 | — |
| Product | 2-(4-Chlorophenyl)-3-[4-(3-diethylaminopropoxy)benzoyl]benzofuran | HCID 21435274 | — |
Reaction Steps
When 2-(p-chlorophenyl)benzofuran is acylated with 4-(3-diethylaminopropoxy)benzoyl chloride hydrochloride by the procedure described in Example 6, the title compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947470 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-738e04f70ed342388574e465ee20c0ee |
| Source note | uspto-grants-1976_03 |