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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49530Generated: October 25, 2026

Hydrogen Bromide → 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide

https://huagongshe.com/reaction/49530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantAcrylamideHCID 6579—
Reactant5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 10903424—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 12094663—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a solution of 2.26 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide in 27 ml of acetone and 11 ml of methanol were added 5.6 ml of 47% solution of hydrobromic acid, 540 mg of sodium nitrite and 2 ml of water under cooling with ice, and the mixture was stirred for 10 minutes. To the reaction mixture were added 3.00 g of acrylamide, and, after heated to 30° C., 135 mg of cupric oxide were added little by little, and the mixture was stirred further for 2 hours at 30° C. Solvent was distilled off under reduced pressure, and 25% aqueous ammonia was added to the residue, which was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in sequence and dried over anhydrous sodium sulfate. Solvent was distilled off under reduced pressure, the residue obtained was crystallized from hexane:ethyl acetate=1:1, and then the crystals were collected by filtration to obtain 1.55 g of 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706763B1
Source datasetuspto-grants-2004_03
ORD IDord-166dbfddd38c4b35b4a216d8319fea93
Source noteuspto-grants-2004_03