HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenyl-benzofuran → HCID 21435342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenyl-benzofuran | HCID 3517936 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzoyl chloride | HCID 3787187 | — |
| Product | HCID 21435342 | HCID 21435342 | — |
Reaction Steps
Acylation of 2-phenylbenzofuran with 3,5-di-t-butyl-4-hydroxybenzoyl chloride as described above gives 3-(3,5-di-t-butyl-4-hydroxybenzoyl)-2-phenylbenzofuran which, upon reaction with 3-diethylaminopropyl chloride and potassium hydroxide in ethanol according to procedures described above, gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024273 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-c81a6e077f7c4e23b7a0d0447d82f138 |
| Source note | uspto-grants-1977_05 |