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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1243661Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-Amino-5-bromo-N-(2-methoxy-benzyl)-benzamide

https://huagongshe.com/reaction/1243661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-MethoxybenzylamineHCID 81292—
EduktMethyl 2-amino-5-bromobenzoateHCID 736224—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
Produkt2-Amino-5-bromo-N-(2-methoxy-benzyl)-benzamideHCID 21930278—

Reaktionsschritte

Under a nitrogen atmosphere, 2-methoxy benzylamine (10 g, 73 mmol) was suspended in anhydrous toluene (30 ml). This suspension was cooled down in ice bath and (2 M) trimethyl aluminum solution in hexanes (36 ml, 72 mmol) was added slowly. The reaction mixture was stirred at room temperature for 1 hour after the completion of the addition. The resulting solution was then cooled in an ice bath and methyl-2-amino-5-bromobenzoate was added in small portions. The reaction was allowed to stir at room temperature overnight. This solution was poured into a pre-cooled solution 2N HCl (300 ml). The solid obtained was collected by filtration and triturated in methanol (50 ml). The solid was collected and dried under high vacuum oven at 65° C. overnight. Pure product was recovered (16 g). 1H NMR (DMSO) δ=3.8 (s, 3H), 4.35 (sd, 2H), 6.5 (2H), 6.6 (1H), 6.85 (1H), 6.9 (1H), 7.1–7.25 (3H), 7.7 (1H), 8.7 (br, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07119120B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-45fb4ab79464446b9138a1a96c3e3d2f
Quellennotizuspto-grants-2006_10