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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393572Erstellt: 23. Oktober 2026

N,N-Diethylaniline → 2-Hydroxy-1-naphthamide

https://huagongshe.com/de/reaction/393572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DiethylanilineHCID 7061—
Edukt2-Hydroxy-1-naphthoic acidHCID 16790—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Hydroxy-1-naphthamideHCID 15105224345,7%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

Diethylaniline (0.27 μL, 1.7 μmol, 1.1 equiv) was added in one portion to a stirred solution of the amine (0.8 mg, 1.5 μmol, 1 equiv) in THF (0.2 mL) at 0° C. under an argon atmosphere and the solution was stirred for 5 min. 2-Hydroxy-1-naphthoic acid (0.37 mg, 2.0 μmol, 1.3 equiv), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.38 mg, 2.0 μmol, 1.3 equiv) and 1-hydroxybenzotriazole (0.25 mg, 1.8 μmol, 1.2 equiv) were then added separately, each in one portion, to the above solution at 0° C. The reaction mixture was warmed to 23° C. over 13 h 20 min, then was quenched with saturated aqueous ammonium chloride solution (3 mL). The mixture was diluted with ethyl acetate (10 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (10 mL) and the combined organic layer was dried over sodium sulfate. Concentration in vacuo left a white solid, which was purified by flash column chromatography (85% ethyl acetate-hexanes) to give the 2-hydroxy-naphthalene-1-carboxylic acid amide derivative (1.1 mg, 100%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06809099B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-3b78a769ebff43a498e45b363e11f4fc
Quellennotizuspto-grants-2004_10