HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → 2,4-Dimethyldiphenylsulfone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Catalyst | Zinc(II) bis-triflimide | HCID 131725279 | — |
| Solvent | HCID 178448536 | HCID 178448536 | — |
| Product | 2,4-Dimethyldiphenylsulfone | HCID 521084 | 99% |
Reaction Steps
Zinc(II) bis-triflimide (0.062 g, 1 mol %) was dissolved in [bmim][NTf2] (1.0 g) in a round-bottomed flask equipped with a magnetic stirrer and reflux condenser and m-xylene (2.12 g, 20 mmol) and benzene sulfonyl chloride (1.76 g, 10 mmol) were added. The mixture was heated under reflux for 18 hours and was analysed by-gas chromatographic analysis as in previous examples. All the benzene sulfonyl chloride had reacted and mostly 2,4-dimethyldiphenylsulfone had formed (yield=99%, 20:1 isomer ratio {by NMR}). The major product is shown below, the structure of the minor isomer is not known but is believed to be the 2,6-dimethyl isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998497B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-14d171ddedb14683b43bdc6d66b34a20 |
| Source note | uspto-grants-2006_02 |