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HRID 577486Erstellt: 24. Oktober 2026

Triethylamine → N-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamide

https://huagongshe.com/de/reaction/577486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt2,2-DiethoxyethylamineHCID 69524—
Edukt3-Methoxy-2-nitrobenzoic acidHCID 78632—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamideHCID 8672371297%

Reaktionsschritte

Oxalyl chloride (34 mL, 0.395 mol) was added to a solution of 3-methoxy-2-nitrobenzoic acid (60 g, 0.305 mol) in dry dichloromethane (600 mL), followed by N,N-dimethylformamide (0.6 mL, 7.8 mmol), which initiates mild gas evolution. The mixture was stirred at room temperature for two hours, then concentrated under vacuum to remove volatiles. The crude acid chloride was dissolved in dry dichloromethane (150 mL) then added dropwise to a cooled (5° C.) solution of aminoacetaldehyde diethylacetal (48 mL, 0.33 mol) and triethylamine (52 mL, 0.374 mol) in dry dichloromethane (250 mL). The mixture was stirred at room temperature for two hours, then washed with saturated aqueous sodium bicarbonate (2×100 mL) and brine (100 mL). The organics were dried over sodium sulfate and concentrated to give N-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamide (296a, 92 g, 97% yield) as a yellow solid. MS: 335 [M+1].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040515B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-3dd1029fa0c342ca8dc5e1dce0bb5721
Quellennotizuspto-grants-2015_05