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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494651Erstellt: 25. Oktober 2026

Hydrochloric Acid → N-(2-hydroxyethyl)-2-methoxy-1-naphthamide

https://huagongshe.com/reaction/494651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolamineHCID 700—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt2-Methoxy-1-naphthoic acidHCID 70356—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-hydroxyethyl)-2-methoxy-1-naphthamideHCID 68871767—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 2-methoxy-naphthalene-1-carboxylic acid (0.50 g, 2.5 mmol) in anhydrous dichloromethane at 0° C. was treated dropwise with a 2.0 M solution of oxalyl chloride in dichloromethane (1.9 mL, 3.8 mmol). The resulting solution was stirred under a N2 atmosphere at 0° C. for 20 min, then allowed to warm to r.t. and stirred 1 hr. The solution was cooled to 0° C., and ethanolamine (0.3 mL, 5.0 mmol) and triethylamine (1.0 mL, 7.2 mmol) were added. The resulting mixture was stirred at 0° C. for 15 min, then allowed to warm to r.t. and stirred 90 min. The mixture was poured into 1N HCl (20 mL) and extracted with dichloromethane (2× 20 mL), and the combined organic layers were washed with saturated NaHCO3 (20 mL) and dried over Na2SO4. The drying agent was filtered off, and the solvent was removed in vacuo to give the title compound as colorless syrup.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538105B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-c786073fdcfa48e9a12116a52788308d
Quellennotizuspto-grants-2009_05