化工社化工社 化学情報印刷レポート · 研究参考用
Potassium Phosphate, Dibasic → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Phosphate, Dibasic | HCID 24450 | — |
| 反応物 | Sodium Persulfate | HCID 62655 | — |
| 反応物 | 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone | HCID 18604772 | — |
| 触媒 | Ferrous sulfate heptahydrate | HCID 62662 | — |
| 触媒 | Cupric acetate monohydrate | HCID 165397 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone | HCID 18604774 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04614614 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-139ed6457cd64e2e9fcb010d4805aeea |
| 出典メモ | uspto-grants-1986_09 |