HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzenesulfonyl chloride → 3-(4-Hydroxyphenylsulfonyl)-2-(4-tolyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | 2-(p-Tolyl)benzofuran | HCID 638458 | — |
| Reactant | 3-(4-Methoxyphenylsulfonyl)-2-(4-tolyl)benzofuran | HCID 22768886 | — |
| Product | 3-(4-Hydroxyphenylsulfonyl)-2-(4-tolyl)benzofuran | HCID 22768875 | — |
Reaction Steps
3-(4-Hydroxyphenylsulfonyl)-2-(4-tolyl)benzofuran is prepared by acylation of 2-(4-tolyl)benzofuran with 4-methoxybenzenesulfonyl chloride followed by demethylation of the 3-(4-methoxyphenylsulfonyl)-2-(4-tolyl)benzofuran thus formed as described hereinabove.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04117128 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-0f92b8fccb4d464da3a1bbaf388ac2f1 |
| Source note | uspto-grants-1978_09 |