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HRID 2372427作成日:2026年10月27日

Sodium Chloride → 2-{1-(4-Phenoxyphenyl)propan-1-ylidene}-1,3-dithiolan

https://huagongshe.com/reaction/2372427

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物HexaneHCID 8058—
反応物3-Phenoxy-1-phenylpropan-1-oneHCID 3876355—
反応物2-Diethoxyphosphoryl-1,3-dithiolaneHCID 13302035—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-{1-(4-Phenoxyphenyl)propan-1-ylidene}-1,3-dithiolanHCID 1990437273%

反応手順

2-Diethoxyphosphoryl-1,3-dithiolan, 3.0 g, was dissolved in 30 ml of tetrahydrofuran and 7.75 ml of 1.6 mole hexane solution of n-butyl lithium was dropwise added to the solution in an argon flow at -65° C. The mixture was stirred at the same temperature for an hour. Then, a solution of 2.55 g of 4-phenoxypropiophenone in 9 ml of tetrahydrofuran was dropwise added to the mixture at the same temperature. The reaction mixture was gradually warmed to room temperature overnight. This suspension was poured onto saturated sodium chloride aqueous solution and the mixture was extracted with chloroform. After drying the chloroform phase over magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (chloroform : hexane =1 : 1) to give 2.60 g of the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05098928
出典データセットuspto-grants-1992_03
ORD IDord-40b7a1c835c347f9958e3d3f188c45bc
出典メモuspto-grants-1992_03