HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzenesulfonyl chloride → HCID 22768858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | HCID 22768889 | HCID 22768889 | — |
| Reactant | 2-{[3-(Trifluoromethyl)phenyl]methyl}-1-benzofuran | HCID 22768895 | — |
| Product | HCID 22768858 | HCID 22768858 | — |
Reaction Steps
Acylation of 2-(3-trifluoromethylbenzyl)benzofuran with 4-methoxybenzenesulfonyl chloride as described in the procedure described above followed by demethylation of the 3-(4-methoxyphenylsulfonyl)-2-(3-trifluoromethylbenzyl)benzofuran thus formed also as described above gives 3-(4-hydroxyphenylsulfonyl)-2-(3-trifluoromethylbenzyl)benzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04117128 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-def9e6f44e5c476289b5eb632c7b77ed |
| Source note | uspto-grants-1978_09 |