関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | (+-)-2-Butanol | HCID 6568 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | (+/-)-2-Propionyl-2-azabicyclo[2.2.1]hept-5-en-3-one | HCID 22673281 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (+/-)-1-Propionylamino-4-hydroxymethyl-2-cyclopentene | HCID 22673282 | 65.3% |
反応手順
16.6 g of (±)-2-propionyl-2-azabicyclo[2.2.1]-hept-5-en-3-one were dissolved in water (140 ml) and 2-butanol (66 ml) under nitrogen and cooled to −5° C. 3 g of sodium borohydride were added in portions over the course of 2 h. The mixture was stirred at 10° C. for 2.5 h and then adjusted to pH 2.2 with a mixture of conc. hydrochloric acid and water (1/1). The solution was evaporated to 40 g and adjusted to pH 6.2 with 2N NaOH. The mixture was extracted with 5×50 ml of dichloromethane. The combined organic phases were completely evaporated, and the residue was recrystallized in toluene (150 ml). 11.1 g of title compound were obtained. The yield was 65%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06262295B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-604ac0b40a2f41e5b39f108b110d5296 |
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| 出典メモ | uspto-grants-2001_07 |
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