関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-(1-Hydroximinoethyl)phenoxathiin | HCID 515182 | — |
| 反応物 | Borane;pyridine | HCID 2723995 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(1-Hydroxaminoethyl)phenoxathiin | HCID 15661013 | 89.9% |
反応手順
The oxime from Step 1 (450 mg, 1.75 mmol) was suspended in ethanol (9 mL) and, at 0° C., there was added pyridine-borane (325 mg, 3.5 mmol) and 4M ethanolic hydrogen chloride (HCl) (1.33 mL, 5.32 mmol). The mixture was stirred at 0° C. for 20 minutes, then at room temperature for 1 hour. The ethanol was evaporated and the residue partitioned between water and ether. The aqueous portion was basified with 1N aqueous sodium hydroxide and extracted twice with ether. Drying of the ether and evaporation afforded the title product (408 mg) as an oil which slowly became a white solid, m.p.: 64°-67° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05036067 |
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| 出典データセット | uspto-grants-1991_07 |
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| ORD ID | ord-e653b95f47a446148c1ae41f2403e257 |
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| 出典メモ | uspto-grants-1991_07 |
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