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HRID 1097274作成日:2026年10月25日

Tetrafluorophthalic anhydride → 1-Ethyl-5-methyl-5-(4,5,6,7-tetrafluoro-1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-2,4,6(1H,3H,5H)-pyrimidinetrione

https://huagongshe.com/reaction/1097274

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrafluorophthalic anhydrideHCID 69545—
反応物5-Amino-1-ethyl-5-methylbarbituric acidHCID 66811052—
溶媒Acetic AcidHCID 176—
生成物1-Ethyl-5-methyl-5-(4,5,6,7-tetrafluoro-1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-2,4,6(1H,3H,5H)-pyrimidinetrioneHCID 24765668—

反応手順

A mixture of 5-amino-1-ethyl-5-methylbarbituric acid (0.28 g, 1.50 mmol) and tetrafluorophthalic anhydride (0.40 g, 1.80 mmol) in glacial AcOH (111 mL) was stirred under reflux for 3 hours. The yellow solution was then allowed to cool down to room temperature and evaporated to dryness under reduced pressure. The oily residue was recrystallized from EtOH to give 1-ethyl-5-methyl-5-(tetrafluorophthalimido)barbituric acid (19f) as white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143252B2
出典データセットuspto-grants-2012_03
ORD IDord-927f2953bb044bc9abc58e88268d6712
出典メモuspto-grants-2012_03