戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 335468作成日:2026年10月26日

Acetone → 1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(phenylmethylidene)hydrazine

https://huagongshe.com/reaction/335468

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Dimethyl SulfateHCID 6497—
反応物Potassium CarbonateHCID 11430—
反応物1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-2-(phenylmethylidene)hydrazineHCID 66691978—
溶媒WaterHCID 962—
生成物1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(phenylmethylidene)hydrazineHCID 66691562—
生成物methyl 2-(2,6-diethyl-4-methylphenyl)-2-oxo-N-(phenylmethylidene)ethanehydrazonateHCID 86689363—

反応手順

To a 25 mL volume three-necked flask, 300 mg of 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-2-(phenylmethylidene)hydrazine ((40-a)-(14)-6), 1.9 ml of acetone, 386 mg of potassium carbonate and 152 mg of dimethyl sulfate were added under a nitrogen atmosphere, and the mixture was stirred at room temperature for 1.5 hours. Water was added to the reaction mixture and the resultant was extracted with ethyl acetate three times. The organic layers were combined and dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography (hexane:ethyl acetate=10:1) to give 261 mg of 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(phenylmethylidene)hydrazine ((40-b)-(15)-5) and 28 mg of methyl 2-(2,6-diethyl-4-methylphenyl)-2-oxo-N-(phenylmethylidene)ethanehydrazonate (compound (x-1)).

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-9648865aac63467e8df579b8fa02b650
出典メモuspto-grants-2014_11