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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49530Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/49530

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktAcrylamideHCID 6579—
Edukt5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 10903424—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetoneHCID 180—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 12094663—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706763B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-166dbfddd38c4b35b4a216d8319fea93
Quellennotizuspto-grants-2004_03