戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 12867作成日:2026年10月24日

Dichloromethane → Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/ja/reaction/12867

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物tert-Butylhydrazine monohydrochlorideHCID 81889—
反応物Sodium AcetateHCID 517045—
反応物Methyl 2-((dimethylamino)methylene)-3-oxobutanoateHCID 53395488—
溶媒EthanolHCID 702—
生成物Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylateHCID 5085323071%

反応条件

温度90 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-5c72efe1e923436eb6ffc65c2c606b2c
出典メモuspto-grants-2010_06