돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1393151생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1393151

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물4-AcetylpyridineHCID 14282—
반응물(Benzyloxycarbonylmethyl)triphenylphosphonium bromideHCID 11214019—
용매Diethyl EtherHCID 3283—
생성물Benzyl 3-(4-pyridyl)-2-butenoateHCID 6711893142.4%

반응 조건

온도70 °C

반응 단계

N,N-Dimethylformamide (33 ml) was added to a mixture of 4-acetylpyridine (2.00 g, 16.5 mmol) and (benzyloxycarbonyl)methyltriphenylphosphonium 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, the external temperature was raised to 70° C., and the whole was stirred 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 1.77 g (42%: mixture of E form and Z form) of benzyl 3-(4-pyridyl)-2-butenoate as a pale yellow oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07345064B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-39cac69df6b04c558be12e135c289b67
출처 메모uspto-grants-2008_03