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HRID 643175作成日:2026年10月24日

Imidazole → 1H-Imidazol-1-ylphenylmethanone

https://huagongshe.com/ja/reaction/643175

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物BifonazoleHCID 2378—
反応物Benzoyl chlorideHCID 7412—
生成物1H-Imidazol-1-ylphenylmethanoneHCID 6631974.7%

反応手順

Bifonazole has also been prepared by benzoylation of imidazole with PhCOCl, yielding 74.7% of 1-benzoylimidazole which is subject to react with Gringnard's reactant 4-PhC6H4MgBr followed by a tosylation and subsequent reduction with sodium cyanoborohydride in hexamethylphosphoramide, to yield 68.2% Bifonazole (Es. Patent 539,345).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE041254E1
出典データセットuspto-grants-2010_04
ORD IDord-033c1b9274df4ed89ae8b57cb0b84483
出典メモuspto-grants-2010_04