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HRID 23781作成日:2026年10月26日

Acetic Acid → Diethyl 1,4-dihydro-4-(2'-ethoxy-3',5'-dinitro-6'-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylate

https://huagongshe.com/reaction/23781

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PiperidineHCID 8082—
反応物Ethyl AcetoacetateHCID 8868—
反応物2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
反応物2-Ethoxy-3,5-dinitro-6-pentadecyl benzaldehydeHCID 22574572—
溶媒1-ButanolHCID 263—
生成物Diethyl 1,4-dihydro-4-(2'-ethoxy-3',5'-dinitro-6'-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylateHCID 10175604—

反応手順

2-Ethoxy-3,5-dinitro-6-pentadecyl benzaldehyde (3.73 g, 8.3 mmol) and ethyl acetoacetate (1.08 g, 8.3 mmol) were dissolved in n-butanol (20 mL). Acetic acid (0.5 g, 8.3 mmol) and piperidine (0.7 g, 8.3 mmol) were added and stirred at room temperature for 3-4 hrs. Ethyl-3-amino crotonate (1.08 g, 8.3 mmol) was then added and refluxed for 10 hrs. n-Butanol was evaporated and reaction mixture was washed with distilled water and extracted with dichloromethane (10 mL). Organic layer was dried over sodium sulfate, evaporated and compound was purified by column chromatography using silicagel (100-200 mesh) with hexane:EtOAc (94:6) solvent system to give diethyl 1,4-dihydro-4-(2′-ethoxy-3′,5′-dinitro-6′-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852742B2
出典データセットuspto-grants-2005_02
ORD IDord-b307ba1dc277422ba293d92cbfe0b0d2
出典メモuspto-grants-2005_02