関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | ethyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate | HCID 16394806 | 72% |
反応手順
To a solution of ethyl 3-acetyl-4-oxopentanoate (synthesized as described D. P. Shrout and D. A. Lightner, Synth. Commun. 20 (1990), 2075) (9.676 g, 51.96 mmol) in ethanol, at 0° C., was added slowly a solution of hydrazine hydrate (2.990 g, 59.75 g) in absolute ethanol. The reaction mixture was warmed to room temperature and stirred for 2 hours. After removing ethanol under vacuum, dichloromethane and water were added to the crude product and the organic layer was separated. The aqueous layer was extracted further with dichloromethane and the combined organic extracts were washed with water. After drying over MgSO4 and evaporation of the solvent under reduced pressure, the pyrazole was isolated as a yellow oil. Yield: 72% (6.777 g, 37.2 mmol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08372379B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-9c886412d52e4145be71feddcd8fb175 |
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| 出典メモ | uspto-grants-2013_02 |
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