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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23781생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/23781

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PiperidineHCID 8082—
반응물Ethyl AcetoacetateHCID 8868—
반응물2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
반응물2-Ethoxy-3,5-dinitro-6-pentadecyl benzaldehydeHCID 22574572—
용매1-ButanolHCID 263—
생성물Diethyl 1,4-dihydro-4-(2'-ethoxy-3',5'-dinitro-6'-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylateHCID 10175604—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852742B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-b307ba1dc277422ba293d92cbfe0b0d2
출처 메모uspto-grants-2005_02