HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzenesulfonyl chloride → 2-(4-Chlorophenyl)-3-(4-hydroxyphenylsulfonyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | 2-(4-Chlorophenyl)-1-benzofuran | HCID 4368312 | — |
| Reactant | 2-(4-Chlorophenyl)-3-(4-methoxyphenylsulfonyl)benzofuran | HCID 22768869 | — |
| Product | 2-(4-Chlorophenyl)-3-(4-hydroxyphenylsulfonyl)benzofuran | HCID 22768898 | — |
Reaction Steps
Acylation of 2-(p-chlorophenyl)benzofuran with 4-methoxybenzenesulfonyl chloride as described in Example 1 followed by demethylation of the 2-(4-chlorophenyl)-3-(4-methoxyphenylsulfonyl)benzofuran thus formed also as described therein, gives 2-(4-chlorophenyl)-3-(4-hydroxyphenylsulfonyl)benzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04117128 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-8033d638734d4ee5bb74eab89d996bdb |
| Source note | uspto-grants-1978_09 |