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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(4-Chlorophenoxy)benzaldehyde | HCID 616015 | — |
| 반응물 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67336952 | 74.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07662965B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-edab8f3343634601be0527e713a2acbf |
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| 출처 메모 | uspto-grants-2010_02 |
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