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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483384Erstellt: 24. Oktober 2026

Ammonia → 3-Phenoxybenzamide

https://huagongshe.com/de/reaction/483384

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktMethyl chloroformateHCID 6586—
EduktTriethylamineHCID 8471—
Edukt3-Phenoxybenzoic acidHCID 19539—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-PhenoxybenzamideHCID 16618625—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Triethylamine (5.6 g) was added at 0° C. under N2 to a stirred solution of 3-phenoxybenzoic acid (10.7 g, Aldrich) in THF (75 ml), followed by the addition of methyl chloroformate (4.7 g) at less than 5° C. After additions were complete, the mixture was stirred at 0° C. for 30 minutes. 0.88 Ammonia (30 ml) was added and the mixture stirred at room temperature for 20 hours, then evaporated in vacuo and the residue taken up in ethyl acetate (100 ml) and water (100 ml). The aqueous phase was separated, extracted with ethyl acetate and the combined ethyl acetate solutions washed with 5% w/v aqu. Na2CO3 (2×50 ml), 2N aqu. HCl (50 ml) and water (100 ml), dried over Na2SO4 and evaporated in vacuo to give the desired product as a colourless solid which was recrystallised from ethyl acetate/60-80 pet. ether (1:2 v/v), mp 125°-127° C. (6.5 g). The 200 MHz 1H NMR was consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05225431
Quelldatensatzuspto-grants-1993_07
ORD IDord-c40945c43d404ed4bbd4ae807c70c784
Quellennotizuspto-grants-1993_07