HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 12629501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | HCID 12629500 | HCID 12629500 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12629501 | HCID 12629501 | 92% |
Reaction Steps
To a solution of methoxymethyl t-butyl sulphide XIV(ii) (2.68 g, 0.020 mol) in MeOH (80 mL) was added a solution of potassium peroxymonosulfate (2 KHSO5 KHSO4 K2SO4, Oxone®) (36.8 g, 0.060 mol) in water (80 mL) at 0° C. The resulting cloudy solution was warmed to room temperature and then stirred overnight. The mixture was diluted with water (30 mL), extracted with EtOAc (3×70 mL), washed with brine, dried over MgSO4, concentrated in vacuo, and then purified by column chromatography (25% EtOAc/hexanes) to give 3.05 g (92%) of Methoxymethyl t-butyl sulfone XII(iii) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ 4.50 (s, 2H), 3.63 (s, 3H), 1.38 (s, 9H); 13NMR (100 MHz, CDCl3) δ 83.19, 60.84, 59.61, 23.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106035B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d76c67e7f3274a72bbe9f8aba5e954f6 |
| Source note | uspto-grants-2012_01 |