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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1701332Erstellt: 25. Oktober 2026

Acetic Acid → 4-(((5-Chloro-2thienyl)methyl)amino)-benzoic acid

https://huagongshe.com/reaction/1701332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt4-Aminobenzoic AcidHCID 978—
EduktN-boranyl-N-methylmethanamineHCID 74604—
Edukt2-Thiophenecarboxaldehyde, 5-chloro-HCID 81700—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt4-(((5-Chloro-2thienyl)methyl)amino)-benzoic acidHCID 20347826—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture containing 46.6 grams (0.34 moles) of p-aminobenzoic acid, 50 grams (0.34 moles) of 5-chloro-2-thiophenecarboxaldehyde and 400 ml. of toluene was heated to reflux for about three and a half hours. The water formed was collected in a Dean-Stark trap. The reaction mass was cooled at the end of this period and the Schiff base collected as a tan solid. To a mixture of the intermediate Schiff base and 1.2 liters of glacial acetic acid 21.2 grams (0.36 moles) of dimethylaminoborane was added. The reaction mass was warmed to 40° C. for about 30 minutes and poured in 2 liters of ice water. The white precipitate of 4-(((5-chloro-2-thienyl)methyl)amino)benzoic acid was washed in water, dried, and recrystallized from toluene. The melting point was 177°-178° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04192884
Quelldatensatzuspto-grants-1980_03
ORD IDord-ad488bf1274642eaaa6e1e919907b224
Quellennotizuspto-grants-1980_03