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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 591724Erstellt: 26. Oktober 2026

4-Methylmorpholine → 2-Amino-4-methoxybenzamide

https://huagongshe.com/reaction/591724

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktAmmonium HydroxideHCID 14923—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt2-Amino-4-methoxybenzoic acidHCID 351010—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Amino-4-methoxybenzamideHCID 14023002—

Reaktionsschritte

To a stirred solution of 2-amino-4-methoxy-benzoic acid (3.00 g, 17.9 mmol) in THF (90 mL), EDCl (7.89 g, 41.1 mmol) and HOBt (7.95 g, 51.9 mmol) were added and stirred at room temperature for 30 minutes. Then, N-methylmorpholine (6.15 g, 60.0 mmol) and aqueous 50% (v/v) NH4OH (12 mL, 171.4 mmol) were added. The mixture was stirred for 16 hours at room temperature. The solvent was removed under reduced pressure and the residue was extracted with ethyl acetate (4×100 mL). The combined organic phase was washed with water, then brine, and dried over anhydrous sodium sulfate. Solvent was evaporated to give 2-amino-4-methoxy-benzamide as an off-white solid. Yield: 1.80 g, (60%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09238640B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-0b7fdd842aa14799a40de6ba58265e20
Quellennotizuspto-grants-2016_01