HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Persulfate → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Persulfate | HCID 24412 | — |
| Edukt | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Edukt | 1-(2,4-dimethoxybenzyl)-3-(S)-hydroxymethyl-4-(R)-tert.butylsulphonyl-2-azetidinone | HCID 18604771 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone | HCID 18604774 | — |
Reaktionsschritte
A solution of 74 mg (0.2 mmol) of 1-(2,4-dimethoxybenzyl)-3-(S)-hydroxymethyl-4-(R)-tert.butylsulphonyl-2-azetidinone (see Example 20), 486 mg (1.8 mmol) of potassium peroxydisulphate and 174 mg (1.0 mmol) of dipotassium hydrogen phosphate in 4 ml of acetonitrile is stirred for 2 hours at 65° under a reflux condenser, the resulting reaction mixture is freed from acetonitrile under reduced pressure and the aqueous residue is extracted with ethyl acetate. After drying of the organic phase over Na2SO4 and concentration by evaporation in vacuo, a residue is obtained from which the title compound is obtained in the form of colourless crystals by adding a little methylene chloride and ether.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04614614 |
| Quelldatensatz | uspto-grants-1986_09 |
| ORD ID | ord-aa853de2f5c04505a7cd89b5973f20c2 |
| Quellennotiz | uspto-grants-1986_09 |