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HRID 2390147생성일: 2026년 10월 25일

3-Bromopyridine-4-carboxaldehyde → 3-Bromo-4-(prop-1-en-1-yl)pyridine

https://huagongshe.com/reaction/2390147

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromopyridine-4-carboxaldehydeHCID 2762997—
반응물3-Bromo-4-(hex-1-en-1-yl)pyridineHCID 67008079—
촉매Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
생성물3-Bromo-4-(prop-1-en-1-yl)pyridineHCID 67008087—

반응 단계

Following the general method as outlined in Intermediate 12, starting from 3-bromo-4-pyridinecarboxaldehyde (Aldrich) and ethyltriphenylphosphonium bromide, the title compound (mixture of cis and trans isomers) was obtained as a colorless liquid after purification by flash column chromatography, eluting with cyclohexane containing increasing amounts of EtOAc.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273769B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-8b3bb53a700c4aa598605a96d7668fee
출처 메모uspto-grants-2012_09