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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12538생성일: 2026년 10월 25일

4-(Trifluoromethyl)benzaldehyde → Ethyl 5-(4-ethylphenyl)-6-(4-(trifluoromethyl)phenyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/12538

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzaldehydeHCID 67996—
반응물3-Ethoxycarbonyl-1,1,1-triphenyl-6-(4-ethylphenyl)-2-aza-1lambda5-phosphahexa-1,3,5-trieneHCID 86619069—
용매AcetonitrileHCID 6342—
생성물Ethyl 5-(4-ethylphenyl)-6-(4-(trifluoromethyl)phenyl)pyridine-2-carboxylateHCID 68407277—

반응 조건

온도60 °C

반응 단계

General Procedure K. 4-(trifluoromethyl)benzaldehyde (153 mg, 1.88 mmol) was added to a stirred solution of 3-ethoxycarbonyl-1,1,1-triphenyl-6-(4-ethylphenyl)-2-aza-1λ5-phosphahexa-1,3,5-triene (Compound 46, 444 mg, 0.88 mmol) in dry acetonitrile (10 ml) and the solution was heated to 60° C. for 18 hours. The solution was concentrated in vacuo, and the crude product was passed through a silica gel column with 15% ethyl acetate in hexane as eluant to give the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728014B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-12e19353160e48d3b4cc4a7e27d8621c
출처 메모uspto-grants-2010_06