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HRID 1195374作成日:2026年10月25日

1,5-Dimethyltetrazole → 1,1-Bis(2-fluoro-4-methylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol

https://huagongshe.com/reaction/1195374

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-DimethyltetrazoleHCID 78825—
反応物2,2'-Difluoro-4,4'-dimethylbenzophenoneHCID 14723981—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Bis(2-fluoro-4-methylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanolHCID 14723992—

反応条件

温度-10 °C

反応手順

To a solution of 1,5-dimethyltetrazole (4.6 g, 4.7 mmoles) in tetrahydrofuran (40 mL) at -50° C. was added butyl lithium solution (21.4 mL of a 2.2M solution, 4.7 mmoles). After stirring for 10 minutes, a solution of 2,2'-difluoro-4,4'-dimethylbenzophenone in tetrahydrofuran (15 mL) was added. The solution was stirred for 2.5 hours during which time it was allowed to warm to -10° C. The reaction was quenched by adding 1N hydrochloric acid. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic fractions were dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and crystallized from isopropyl acetate to give 8.0 g of the title compound; m.p.=150°-151° C. MS: M+ =344.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05110940
出典データセットuspto-grants-1992_05
ORD IDord-6e6ed3e629fa445287a8fa9a3fe0ead4
出典メモuspto-grants-1992_05