HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (4 t-Butylphenylsulphonyl)nitromethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | (4-t-Butylphenylthio)nitromethane | HCID 14404080 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4 t-Butylphenylsulphonyl)nitromethane | HCID 14404081 | — |
Reaction Steps
A solution of potassium peroxymonosulphate [`Oxone` (trade mark); 38.7 g, 63 mmol]in water (100 ml) was added in one portion to a vigorously stirred solution of (4-t-butylphenylthio)nitromethane (A) (4.76 g, 21.9 mmol) in methanol (90 ml). A cream coloured precipitate was formed. The mixture was stirred overnight. Water (200 ml) was then added and the mixture was extracted with ethyl acetate. The extracts were combined, dried (MgSO4) and the solvent was removed by evaporation. The residual yellow solid was recrystallised from cyclohexane to give (4 t-butylphenylsulphonyl)nitromethane, as a colourless solid (3.34 g), m.p. 90°-91° C., microanalysis found: C, 51.4; H, 5.9; N, 5.4%; C11H15NO4S: requires: C, 51.4; H, 5.9; N, 5.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153227 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-c2ebd40050344b869d0cf8bec5195fba |
| Source note | uspto-grants-1992_10 |