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HRID 2422255作成日:2026年10月26日

Dimethylformamide → 3-(1-Phenylvinyl)benzaldehyde

https://huagongshe.com/reaction/2422255

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ammonium ChlorideHCID 25517—
反応物1-Bromo-3-(1-phenylethenyl)benzeneHCID 23083178—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物3-(1-Phenylvinyl)benzaldehydeHCID 1310274678%

反応手順

A solution of 1-bromo-3-(1-phenylvinyl)benzene (1.00 g, 3.86 mmol) in tetrahydrofuran (5 mL) was stirred under a nitrogen atmosphere at −78° C., and 1.6 M n-butyllithium/hexane solution (3 mL, 4.8 mmol) was added dropwise. After 1 hr, N,N-dimethylformamide (0.372 mL, 4.80 mmol) was added, and the mixture was further stirred at the same temperature for 2 hrs. Aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-20% ethyl acetate/hexane) to give the title compound (0.626 g, yield 78%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960369B2
出典データセットuspto-grants-2011_06
ORD IDord-941befe5b50a4bd3a22e0dda6c60842f
出典メモuspto-grants-2011_06