HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Phosphate, Dibasic → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | Sodium Persulfate | HCID 62655 | — |
| Reactant | 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone | HCID 18604772 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone | HCID 18604774 | — |
Reaction Steps
A solution of 68.3 mg (0.2 mmol) of 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone in 4 ml of acetonitrile is added to a solution of 428 mg (1.8 mmol) of sodium peroxydisulphate, 174 mg (1 mmol) of dipotassium hydrogen phosphate, 1 mg of iron(II) sulphate heptahydrate and 2 mg of copper(II) acetate hydrate in 4 ml of water. The mixture is stirred for 2 hours under an argon atmosphere at a bath temperature of 65°. The resulting mixture is then concentrated to half its volume under reduced pressure and extracted with ethyl acetate. The extract is triturated with methylene chloride and ether and the pure title compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04614614 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-139ed6457cd64e2e9fcb010d4805aeea |
| Source note | uspto-grants-1986_09 |