HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-Butyl-5-nitrobenzofuran | HCID 9837358 | — |
| Product | (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone | HCID 22595055 | — |
Reaction Steps
reaction of 2-butyl-5-nitrobenzofuran with anisoyl chloride in the presence of tin tetrachloride based on the Friedel-Crafts reaction conditions and hydrolysis to form 2-butyl-3-(4-methoxybenzoyl)-5-nitrobenzofuran,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06828448B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-6c6ddfd7e1224ac3ad3fe32aa13cc310 |
| Source note | uspto-grants-2004_12 |