HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfite → HCID 19605313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 9884329 | HCID 9884329 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19605313 | HCID 19605313 | 27% |
Reaction Steps
A solution of 4-(benzylthio)-1-(4-phenyl-2-oxobutyl)azetidin-2-one (3.1 g, 9.2 mmol) in dichloromethane (100 ml) was cooled to -50 to -60° C. and a solution of m-chloroperbenzoic acid (1.9 g, 11 mmol) in dichloromethane (80 ml) added dropwise with stirring over 30 min. After a further 30 min at -50 to -60° C. the reaction mixture was shaken with a mixture of saturated aqueous sodium sulphite and saturated sodium hydrogen carbonate and the organic layer separated, dried (MgSO4) and evaporated to a solid. Two recrystallisations from ethyl acetate gave (4R,SR/4S,SS) 4-(benzylsulphinyl)-1-(4-phenyl-2-oxobutyl)azetidin-2-one (0.8 g, 27%), mp 147-9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990102 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-8042ac6d203a4b4989dd43a36618c7db |
| Source note | uspto-grants-1999_11 |