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HRID 330676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/330676

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 -=° 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US04897490
出典データセットuspto-grants-1990_01
ORD IDord-3bbc23d6d833405b89f613091775c579
出典メモuspto-grants-1990_01