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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27462Erstellt: 23. Oktober 2026

4-(2-Acetamidoethyl)benzoic acid → 3-Aminobenzoic Acid

https://huagongshe.com/de/reaction/27462

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(2-Acetamidoethyl)benzoic acidHCID 343701—
Edukt4-(2-Acetaminoethyl)-3-nitro-benzoic acidHCID 23343064—
LösungsmittelMethanolHCID 887—
Produkt3-Aminobenzoic AcidHCID 7419—

Reaktionsschritte

4-(2-Acetaminoethyl)-benzoic acid was reacted with nitrating acid to 4-(2-acetaminoethyl)-3-nitro-benzoic acid, M.p. 189° C. (from methanol). The following catalytical hydrogenation yielded the 4-(2-acetaminoethyl)-3-aminoethyl)-3-amino-benzoic acid with a melting point of 143° C. (from ethanol/petroleum ether). From this compound, there was obtained by diazotation and Sandmeyer-reaction the 4-(2-acetamino-ethyl)-3-chloro-benzoic acid having a melting point of 150° C. or by boiling up the diazo solution, the 4-(2-acetaminoethyl)-3-chloro-benzoic acid M.p. 222°-223° C. From 4-(2-acetaminoethyl)-3-hydroxy-benzoic acid, there were obtained with dimethyl sulfate or diethyl sulfate, the corresponding 4-(2-acetaminoethyl)-3-methoxy-benzoic acid methyl ester and the 4-(2-acetaminoethyl)-3-ethoxy-benzoic acid ethyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221815
Quelldatensatzuspto-grants-1980_09
ORD IDord-981300d1e03941baa7f21a3dc6806230
Quellennotizuspto-grants-1980_09