Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | HCID 19764842 | HCID 19764842 | — |
| Product | HCID 19764854 | HCID 19764854 | 82% |
Reaction Steps
A solution of potassium peroxymonosulphate (17.7 g) in water (30 ml) was added to a mixture of 3-bromophenyl 2-naphthyl sulphide (3 g) and ethanol (30 ml) which had been cooled to 0° C. in an ice-bath. The mixture was stirred at ambient temperature for 18 hours and at 60° C. for 5 hours. The mixture was cooled to ambient temperature and partitioned between chloroform and water. The organic phase was dried (MgSO4) and evaporated to give 3-bromophenyl 2-naphthyl sulphone (2.7 g, 82%) as a solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137913 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-6d64755f2000405a8e103af310aea8e7 |
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| Source note | uspto-grants-1992_08 |
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