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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18390생성일: 2026년 10월 25일

Dimethylformamide → Benzyl 3-(4-pyridyl)-2-butenoate

https://huagongshe.com/reaction/18390

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물4-AcetylpyridineHCID 14282—
반응물(Benzyloxycarbonyl)triphenylphosphonium bromideHCID 23024669—
용매Diethyl EtherHCID 3283—
생성물Benzyl 3-(4-pyridyl)-2-butenoateHCID 6711893142%

반응 단계

N,N-Dimethylformamide (33 ml) was added to a mixture of 4-acetylpyridine (2.00 g, 16.5 mmol) and (benzyloxycarbonyl)triphenylphosphonium bromide (8.94 g, 18.2 mmol), and the whole was stirred under ice-cooling. Potassium carbonate (9.12 g, 66.0 mmol) was added thereto, and the whole was stirred at an external temperature of 70° C. overnight. The reaction mixture was diluted with diethyl ether (100 ml), and the whole was washed with water (100 ml, twice) and saturated brine (50 ml) successively. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give benzyl 3-(4-pyridyl)-2-butenate (1.77 g, 42%: mixture of E body and Z body) as a pale yellow oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741346B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-eae2e1c8cc89488595a923339b143a1c
출처 메모uspto-grants-2010_06