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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methoxybenzylamine | HCID 81292 | — |
| Reactant | Methyl 2-amino-5-bromobenzoate | HCID 736224 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Amino-5-bromo-N-(2-methoxy-benzyl)-benzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119120B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-45fb4ab79464446b9138a1a96c3e3d2f |
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| Source note | uspto-grants-2006_10 |
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