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HRID 335413作成日:2026年10月24日

Acetic Acid → 1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazine

https://huagongshe.com/ja/reaction/335413

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TetrahydrofuranHCID 8028—
反応物1-Methylthio-2-propanoneHCID 6430713—
反応物2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetohydrazideHCID 56942873—
溶媒WaterHCID 962—
生成物1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazineHCID 8668934581.4%

反応手順

To a 200 ml volume four-necked flask, 2-(2,6-diethyl-4-methylphenyl)-2-oxoacetohydrazine ((12-1)-(11)-39) (6.44 g), tetrahydrofuran (72 ml), and acetic acid (1.65 g) were added under a nitrogen atmosphere. 1-methylsulfanyl-2-propanone (7-0-1) (3.12 g) was added at room temperature, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture was added water (30 ml), and extracted with tert-butyl methyl ether. The organic layer was concentrated under reduced pressure to give 7.17 g of 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-2-(1-methylsulfanyl-2-propylidene)hydrazine ((4-4)-(8)-39).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08884010B2
出典データセットuspto-grants-2014_11
ORD IDord-f22862d887c94aacbe6b1121c774211b
出典メモuspto-grants-2014_11