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HRID 405692作成日:2026年10月24日

Triphenylphosphine → 1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanone

https://huagongshe.com/ja/reaction/405692

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Sodium BicarbonateHCID 516892—
反応物2-Bromo-1-(4-bromo-3-methylphenyl)ethanoneHCID 59166346—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanoneHCID 86674671—

反応手順

1300 mg of 2-Bromo-1-(4-bromo-3-methyl-phenyl)-ethanone (VIIa) (Journal of Organic Chemistry (1947), 12, 617-703) was stirred with 1300 mg of triphenylphosphine in 20 ml of dichloromethane at ambient temperature for 18 hours. The mixture was diluted with toluene and the separated phosphonium salt was filtered off. It was then suspended in 20 ml of dichloromethane and 20 ml of water. 800 mg (7.55 mmol) of sodium bicarbonate was then added in 20 ml of water and the mixture was stirred overnight. The organic layer was separated, dried and evaporated under reduced pressure. The residue was triturated with hexane giving 1.6 g (86%) of 1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanone (Va) as a solid. 1H-NMR (CDCl3, δ in ppm): 7.40-7.90 (m, 18H), 4.40 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754053B2
出典データセットuspto-grants-2014_06
ORD IDord-378b5957ca814ec68c328221864c4604
出典メモuspto-grants-2014_06