HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylcatechol → 4-(4-Chloro-3-nitrophenylsulphonyl)-5-methyl-1,2-benzenediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylcatechol | HCID 9958 | — |
| Reactant | 4-Chloro-3-nitrobenzenesulfinic acid | HCID 4097544 | — |
| Product | 4-(4-Chloro-3-nitrophenylsulphonyl)-5-methyl-1,2-benzenediol | HCID 23312083 | — |
Reaction Steps
66 g (297.8 mmol) of 4-chloro-3-nitrobenzenesulphinic acid (produced by reduction of 4-chloro-3-nitrobenzenesulphonyl chloride with sodium sulphite) are condensed with 41.95 g (337.9 mmol) of 4-methyl-1,2-benzenediol in a manner analogous to that described in Example 4, yielding 4-(4-chloro-3-nitrophenylsulphonyl)-5-methyl-1,2-benzenediol in the form of crystals having a melting point of 196°-197° (from ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04600709 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-84065377be804fb49823923b6813b87c |
| Source note | uspto-grants-1986_07 |