HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → HCID 86734036, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | HCID 21435285 | HCID 21435285 | — |
| Reactant | 1-tert-Butyl-3-(chloromethyl)azetidine | HCID 21510497 | — |
| Reactant | 2-Benzyl-5-bromo-1-benzofuran | HCID 22768909 | — |
| Product | HCID 86734036 | HCID 86734036 | — |
Reaction Steps
2-Benzyl-5-bromobenzofuran is acylated with p-anisoyl chloride as described above, the resulting 2-benzyl-5-bromo-3-(4-methoxybenzoyl)benzofuran is dimethylated and the product thus formed is reacted with N-t-butyl-3-chloromethylazetidine as described in Example 3 to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983245 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-40c0d73d8e344325931b012958e995ae |
| Source note | uspto-grants-1976_09 |