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 | — |
| Reactant | 1-Butyl-3-methylimidazolium | HCID 2734162 | — |
| Catalyst | Zinc(II) bis-triflimide | HCID 131725279 | — |
| 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 | US07781625B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-2dee0ecbec004775a240ba780a38d605 |
| Source note | uspto-grants-2010_08 |