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HRID 613683作成日:2026年10月24日

4-Chlorobutyrophenone → 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide

https://huagongshe.com/ja/reaction/613683

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobutyrophenoneHCID 253533—
反応物Hydrazinecarbothioamide, N-phenyl-HCID 730679—
溶媒EthanolHCID 702—
生成物2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamideHCID 5374726062.6%

反応手順

A mixture of 4-chlorobutyrophenone (6.7 mL, 42 mmol) and 4-phenyl-3-thiosemicarbazide (7.0 g, 42 mmol) in 500 mL of ethanol was warmed under a nitrogen atmosphere to dissolve all the solids and then the reaction stirred at room temperature for four days. The solid formed was collected by filtration and dried under reduced pressure to give 8.73 g of a white solid. Recrystallization of the solid from ethanol gave 7.99 g (57%) of the title compound as a white solid, mp 107-109° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06008362
出典データセットuspto-grants-1999_12
ORD IDord-a4ace6d1b5ed443c8dd624f2fd2543b9
出典メモuspto-grants-1999_12