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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1444745생성일: 2026년 10월 26일

3-(4-Chlorophenoxy)benzaldehyde → 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride

https://huagongshe.com/reaction/1444745

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
반응물3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
용매IsopropanolHCID 3776—
생성물3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 6733695274.1%

반응 조건

온도80 °C

반응 단계

3-(5-Ammoniopentanoyl)pyridinium chloride (162 mg, 0.64 mmol) was suspended in a reaction vessel with i-propanol (12 mL). 3-(4-chlorophenoxy)benzaldehyde (225 mg, 0.97 mmol) was then added and the reaction vessel sealed. The reaction was heated to 80° C. overnight and then cooled to room temperature. The precipitate was recovered by vacuum filtration, washed with a 20% i-propanol in hexane solution then dried under vacuum giving 161 mg (56%) of a tan-colored solid. LC-MS: RT=6.22 min, [M+H]+=375.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07662965B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-edab8f3343634601be0527e713a2acbf
출처 메모uspto-grants-2010_02