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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1678319Erstellt: 26. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Fluorobiphenyl-4-carboxaldehydeHCID 2759083—
Edukt3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
Produkt3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 6733915273,8%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08008499B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-e639822e32474c44869eaf9ee34e3778
Quellennotizuspto-grants-2011_08