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HRID 2399778作成日:2026年10月25日

3-Chlorothiophenol → 4-Chlorophenyl-alpha-[(3-chlorophenyl)thiomethyl]acetic acid

https://huagongshe.com/reaction/2399778

反応式

関与物質

役割名称HCID仕込み量
反応物3-ChlorothiophenolHCID 16257—
反応物Benzeneacetic acid, 4-chloro-alpha-methylene-, ethyl esterHCID 181005—
触媒Sodium ethoxideHCID 2723922—
溶媒EthanolHCID 702—
生成物4-Chlorophenyl-alpha-[(3-chlorophenyl)thiomethyl]acetic acidHCID 1938469681.2%

反応手順

A solution of the ethyl 4-chlorophenyl-α-methyleneacetate (4.2 g), m-chlorothiophenol (2.9 g) and sodium ethoxide (0.05 g) in ethanol (20 ml) was stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure, followed by addition of water (150 ml) to the residue, and the mixture was extracted with ether (150 ml). The extract was washed two times with 15% aqueous sodium hydroxide, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. To the resulting residue were added 88% formic acid (20 ml) and methanesulfonic acid (2.1 ml), followed by heating at reflux for 8 hours. After cooling to room temperature, the mixture was poured into water (100 ml) and extracted with dichloromethane (150 ml). The aqueous layer was further washed with dichloromethane (50 ml), and the combined organic layer was dried over anhydrous magnesium sulfate and concentrated. The resulting residue was subjected to chromatography on silica gel to give 4-chlorophenyl-α-[(3-chlorophenyl)thiomethyl]-acetic acid (yield, 5.3 g), nD23.6, 1.5627

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05451607
出典データセットuspto-grants-1995_09
ORD IDord-7ddebfc6fe294e0cb6cb7a947d540cfe
出典メモuspto-grants-1995_09