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HRID 15400作成日:2026年10月27日

Diisopropylamine → 2-Bromo-6-fluorobenzaldehyde

https://huagongshe.com/reaction/15400

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物TetrahydrofuranHCID 8028—
反応物1-Bromo-3-fluorobenzeneHCID 14082—
反応物Ammonium ChlorideHCID 25517—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-6-fluorobenzaldehydeHCID 22473977—

反応手順

To a solution of diisopropylamine (2.65 mL) in tetrahydrofuran (30 mL) was added n-butyllithium (2.44 mol/L n-hexane solution, 7.03 mL) at −78° C. under an argon atmosphere, and the mixture was stirred at the same temperature for 5 minutes. To the reaction mixture was added 3-bromofluorobenzene (3 g), and the mixture was stirred at the same temperature for 1 hour. To the reaction mixture was added N,N-dimethylformamide (1.45 mL), and the mixture was stirred at the same temperature for 10 minutes, then a saturated ammonium chloride aqueous solution was added to the reaction mixture, and the mixture was stirred under ice-cooling for 5 minutes. The mixture was poured into water, and the mixture was extracted with diethyl ether. The extract washed with water and brine and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give the title compound (3.43 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732596B2
出典データセットuspto-grants-2010_06
ORD IDord-9b32939980df43e6b1eb49e473bef3e4
出典メモuspto-grants-2010_06