関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Methyl 2-((dimethylamino)methylene)-3-oxobutanoate | HCID 53395488 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate | HCID 50853230 | 71% |
反応手順
A solution of 2-dimethylaminomethylene-3-oxo-butyric acid methyl ester (7.43 g, 43.40 mmol) in absolute ethanol (70 mL) was treated with tert-butylhydrazine hydrochloride (5.52 g, 44.29 mmol) and sodium acetate (4.42 g, 53.88 mmol). The resulting mixture was heated to 90° C. for 18 h. At this time, the reaction was cooled to 25° C. The reaction was poured onto ice using dichloromethane to assist the transfer (50 mL). The mixture was transferred to a separatory funnel at which time the layers were shaken and separated. The aqueous layer was further extracted with dichloromethane (1×50 mL). The combined organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. ISCO CombiFlash (120 g column; 0-10% ethyl acetate/hexanes) afforded 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid methyl ester (6.04 g, 71%) as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728029B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-5c72efe1e923436eb6ffc65c2c606b2c |
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| 出典メモ | uspto-grants-2010_06 |
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