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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241524Generated: October 26, 2026

Water → 4-bromo-3-methyl-N-(trimethylsilylmethyl)benzamide

https://huagongshe.com/reaction/241524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-Bromo-3-methylbenzoic acidHCID 82131—
Reactant1-(Trimethylsilyl)methylamineHCID 87488—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-bromo-3-methyl-N-(trimethylsilylmethyl)benzamideHCID 6683646994%

Reaction Steps

To a suspension of 4-bromo-3-methylbenzoic acid (25 g) and 4-(dimethylamino)pyridine (“DMAP”, 2.1 g) in CH2Cl2 (320 mL) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (“EDC”, 22.4 g) portionwise. Then, (aminomethyl)trimethylsilane (8.6 mL) was added, while cooling to keep the internal temperature below 20° C. The reaction was stirred at room temperature overnight. Water was added under vigorous stirring, and the layers were separated. The aqueous layer was extracted twice with CH2Cl2, and the combined organic phase dried (Na2SO4), and filtered over silica gel using CH2Cl2 and methyl tert-butyl ether (MTBE) to afford the title compound (32.8 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653000B2
Source datasetuspto-grants-2014_02
ORD IDord-84bff735b8e84773b38a246cec69f299
Source noteuspto-grants-2014_02