HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl phenyl sulphide → Benzyl phenyl sulfoxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl phenyl sulphide | HCID 13255 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl phenyl sulfoxide | HCID 239581 | 110.7% |
Reaction Steps
To a solution of benzyl phenyl sulfide (Aldrich; 1.068 g, 5.33 mmol) in 25 mL of CH2Cl2 at −78° C. was slowly added a solution of m-chloroperbenzoic acid (Aldrich, 50-60%; 760 mg, 2.64 mmol if 60%) in 10 mL of CH2CL2. After warming to room temperature and stirring overnight, the solution was added to 20 mL of a saturated NaHCO3 solution. The aqueous layer was separated and extracted with CH2Cl2 (2×10 mL). The pooled organic layers were then dried (MgSO4) and concentrated. The residue was subjected to flash column chromatography (silica gel, 10% acetone/hexane and 15% acetone/hexane) affording the sulfoxide (632 mg, 55%) as a white solid, mp 123-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277838B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-aa269e45cf0a4dc79824a237ba086798 |
| Source note | uspto-grants-2001_08 |