HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1444745Erstellt: 25. Oktober 2026
3-(4-Chlorophenoxy)benzaldehyde → 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride
https://huagongshe.com/reaction/1444745
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-(4-Chlorophenoxy)benzaldehyde | HCID 616015 | — |
| Edukt | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67336952 | 74,1% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07662965B2 |
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| Quelldatensatz | uspto-grants-2010_02 |
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| ORD ID | ord-edab8f3343634601be0527e713a2acbf |
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| Quellennotiz | uspto-grants-2010_02 |
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