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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217909Erstellt: 24. Oktober 2026

Ammonia → 4-(4-Methoxyphenyl)butanamide

https://huagongshe.com/de/reaction/217909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktCarbon DioxideHCID 280—
EduktMethanolHCID 887—
EduktSodium ChlorideHCID 5234—
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
Edukt4-(4-Methoxyphenyl)butyric acidHCID 78280—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(4-Methoxyphenyl)butanamideHCID 22566175—

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

4-(4-Methoxyphenyl) butyric acid (1) (450 g, 2.32 mole) was combined with dry THF (4 L) and 4-methylmorpholine (268 mL, 2.43 mole) in a 12 L three neck flask with mechanical stirring, an ice-methanol cooling bath and nitrogen atmosphere. Small pieces of dry ice were used to bring the bath temperature below −20° C. Isobutyl chloroformate was added at a rate so as not to exceed an internal temperature of −10° C. After stirring for 30 min. at −10 to −20° C., a 4.7 M solution of ammonia in methanol (990 mL, 4.64 mole) was added in one portion. During the addition, the reaction temperature rose to 0° C. The reaction was allowed to stir for 30 min. and then allowed to stand overnight. The product mixture was transferred to a 22 L separatory funnel with ethyl acetate (6 L), and 10% sodium chloride solution (1.5 L). The layers were separated and the organic solution was washed with 10% sodium chloride solution (4×1 L) and then brine (3×500 mL). The organic layer was dried over sodium sulfate, filtered, evaporated and placed under high vacuum overnight. This afforded 432 g (97%) of the pure amide (117) as an off white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198286B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-d785aa70ceed406db48bb0a054bfb2c2
Quellennotizuspto-grants-2012_06