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HRID 262128作成日:2026年10月25日

Ethanone, 2-chloro-1,2-diphenyl- → 2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazole

https://huagongshe.com/reaction/262128

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanone, 2-chloro-1,2-diphenyl-HCID 95343—
反応物2H-1,3-benzodioxole-5-carbothioamideHCID 2776126—
溶媒EthanolHCID 702—
生成物2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazoleHCID 2034498367.1%

反応手順

Thiopiperonylamide (18.1g, 0.10 mole) and desyl chloride (23.1g, 0.10 mole) are heated under reflux in 95% ethanol (100 ml) for two hours. An oil precipitates which solidifies when the reaction mixture is cooled. The solid is collected and recrystallized from ethanolethyl acetate to give 24.0g (67% yield) of 2-(3,4-methylenedioxyphenyl)-4,5-diphenylthiazole, m.p. 121°-124° C. Thiopiperonylamide is also prepared from the corresponding nitrile by the method of Fairfull et al., J. Chem. Soc. 1952, 742.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04153703
出典データセットuspto-grants-1979_05
ORD IDord-e5b0204e8488451689e553449c72c4ac
出典メモuspto-grants-1979_05