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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22922Erstellt: 23. Oktober 2026

Pyridine → 3-(3-Chloro-4-methoxyphenyl)propan-1-amine

https://huagongshe.com/de/reaction/22922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktSulfuryl chlorideHCID 24648—
Edukt4-MethoxybenzaldehydeHCID 31244—
Produkt3-(3-Chloro-4-methoxyphenyl)propan-1-amineHCID 1227768777%

Reaktionsschritte

4-Methoxy-benzaldehyde (Aldrich) (42 g, 0.31 mole) and pyridine (0.6 ml, catalytic) were stirred together under nitrogen and sulfuryl chloride (51 g, 0.37 mole) added over 30 min, maintaining the internal temperature of the reaction at between 25 and 30° C. There was a vigorous evolution of gas. The mixture was stirred at room temperature for a further 30 min, and then warmed to 70° C. for 4 h. Excess reagents were removed by evaporation in vacuo and the residue taken up in 50 ml diisopropyl ether and poured onto 500 ml hexane with vigorous stirring, from which the product precipitates. The solid was filtered off and washed with hexane and then dried in vacuo to give the title product (40.3 g, 77%), m.p. 55-56° C.; 1HNMR (400 MHz, CDCl3) δ: 3.99 (s, 3H), 7.05 (dd, 1H), 7.91 (d, 1H), 9.86 (s, 1H); Anal. Found: C, 56.13; H, 4.14%. C8H7ClO2 requires C, 56.33; H, 4.14%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849649B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-ed79363d7c4b4e89bde6a718f51e6b66
Quellennotizuspto-grants-2005_02