HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → HCID 18611327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | HCID 131715436 | HCID 131715436 | — |
| Product | HCID 18611327 | HCID 18611327 | — |
Reaction Steps
Ozone is passed through a solution of 6.2 g of 2-[4-acetoxy-(3R)-3-[1(R)-fluorethyl]-2-oxoazetidine-1-yl]-3-methyl-2-butenoic acid.benzhydrylester at -78° until a permanent blue colour is achieved. The excess ozone is drive out with nitrogen and 1.75 g of dimethylsulphide added. The reaction mixture is allowed to rise to room temperature. The solvent is evaporated on a rotary evaporator, the residue taken up in 100 ml of methanol and after addition of 2 drops of triethylamine stirred for 2 hours. After renewed concentration the residue is chromatographed on silica gel (dichloromethane/ethylacetate=10/3) to obtain the oily title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04720491 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-5812d03d115e4ba483aa1fff2eb242c5 |
| Source note | uspto-grants-1988_01 |