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HRID 51221作成日:2026年10月23日

Dichloromethane → 2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one

https://huagongshe.com/ja/reaction/51221

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物4-ChloroanilineHCID 7812—
反応物Triethyloxonium tetrafluoroborateHCID 2723982—
反応物5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-oneHCID 12056392—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-oneHCID 1205639957.8%

反応手順

5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (0.28 g) was mixed with a 1M methylene chloride solution of triethyloxonium tetrafluoroborate (1 ml) at room temperature. The reaction mixture was stirred for 24 hrs at room temperature then p-chloroaniline (0.25 g) in chloroform (10 ml) was added to the mixture at 0° C. The mixture was stirred at room temperature for 1 hr and then water was added. The separated oil was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (chloroform-n-hexane, 1/1) to yield 2-(4-chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one (0.21 g) having a melting point of 53-54° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713629B2
出典データセットuspto-grants-2004_03
ORD IDord-cd27c9acc26c47ba8554b42114b3e20a
出典メモuspto-grants-2004_03