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HRID 542798作成日:2026年10月27日

Tetrahydrofuran → 1-(4-fluoro-2-methylaminophenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanone

https://huagongshe.com/reaction/542798

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物1,5-DimethyltetrazoleHCID 78825—
反応物Methyl 4-fluoro-2-(methylamino)benzoateHCID 13474393—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
生成物1-(4-fluoro-2-methylaminophenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanoneHCID 13474394—

反応手順

A solution of butyl lithium in hexane (50 ml of 1.6M solution) was added slowly to a stirred mixture of 1,5-dimethyltetrazole (7.84 g) and dry tetrahydrofuran (170 ml) at 0°-5° under nitrogen. The mixture was stirred at 0°-5° for 0.5 hour and then methyl 4-fluoro-2-methylaminobenzoate (4.84 g) was added in portions at 0°-5°. The mixture was stirred at room temperature for 3 hours and then poured into water (500 ml). The resulting mixture was extracted with dichloromethane (5×60 ml). The extract was dried and evaporated to give an oil which partially solidified overnight. The solid was collected by filtration, washed with toluene and dried in vacuo to give the novel compound 1-(4-fluoro-2-methylaminophenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanone, m.p. 132°-134°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04659718
出典データセットuspto-grants-1987_04
ORD IDord-7340d66b0e6e414fb721ae3a56ac4fc4
出典メモuspto-grants-1987_04