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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243661Generated: October 26, 2026

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

https://huagongshe.com/reaction/1243661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-MethoxybenzylamineHCID 81292—
ReactantMethyl 2-amino-5-bromobenzoateHCID 736224—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
Product2-Amino-5-bromo-N-(2-methoxy-benzyl)-benzamideHCID 21930278—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119120B2
Source datasetuspto-grants-2006_10
ORD IDord-45fb4ab79464446b9138a1a96c3e3d2f
Source noteuspto-grants-2006_10