HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → 4-Methoxy-2,3,6-trimethylbenzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 2,3,5-Trimethylanisole | HCID 88555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxy-2,3,6-trimethylbenzenesulfonyl chloride | HCID 562787 | — |
Reaction Steps
In 500 ml of methylenchloride was dissolved 4.5 g of 2,3,5-trimethylanisole, and after cooling at -5°~-10° C., a solution (400 ml) of 6.0 ml of chlorosulfonic acid in methylene chloride was added dropwise to the mixture. The reaction mixture was kept at room temperature and then poured into ice-5% aqueous NaHCO3. The methylene chloride layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was crystallized from n-hexane and filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04487726 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-d3ead4adc2794510a0bb27b474514578 |
| Source note | uspto-grants-1984_12 |