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HRID 588369作成日:2026年10月27日

Ethanol → ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/588369

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Oxalyl chlorideHCID 65578—
反応物4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acidHCID 673687—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylateHCID 6013669889%

反応手順

4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid (301.68 g, 1.2 moles) was slurried in 1.2 L of DCM and DMF (2.3 g, 31 mmol) followed by addition of oxalyl chloride (115 mL, 1.3 moles) over 37 minutes and then stirred at room temperature for 3 h. To the resulting solution was added EtOH (750 mL, 12.9 mol) over 5 min followed by stirring at room temperature for 2 h. The crude product solution was concentrated to dryness in vacuo and then reconstituted in 1.2 L of warm heptane followed by filtration. The filtrate was concentrated by removing 500 mL of heptane, resulting in precipitation of solids. The solids were collected via filtration and dried to afford ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate as a white solid (297.6 g, 89% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227956B2
出典データセットuspto-grants-2016_01
ORD IDord-884fe9457511462fa089a6eb1ba3a546
出典メモuspto-grants-2016_01