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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1678319생성일: 2026년 10월 27일

2-Fluorobiphenyl-4-carboxaldehyde → 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride

https://huagongshe.com/reaction/1678319

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluorobiphenyl-4-carboxaldehydeHCID 2759083—
반응물3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
촉매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
생성물3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 6733915273.8%

반응 조건

온도85 °C

반응 단계

3-(5-Ammoniopentanoyl)pyridinium chloride (150 mg, 0.60 mmol) and 2-fluorobiphenyl-4-carboxaldehyde (155 mg, 0.78 mmol) were combined in a reaction vessel and treated with ethanol (10 mL) and concentrated HCl(aq) (5 drops). The vessel was then sealed and the reaction was heated to 85° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure then partially dissolved into hot isopropanol. This mixture was left to cool and crystals formed. The crystals were recovered by vacuum filtration, washed with fresh isopropanol, and dried under vacuum giving 92 mg (36%) of a yellow solid. LC-MS: RT=5.88 min, [M+H]+=343.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008499B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-e639822e32474c44869eaf9ee34e3778
출처 메모uspto-grants-2011_08