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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47815Erstellt: 24. Oktober 2026

1-Heptanamine → 2-(4-bromo-phenyl)-N-heptyl-acetamide

https://huagongshe.com/de/reaction/47815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HeptanamineHCID 8127—
EduktThionyl ChlorideHCID 24386—
EduktBenzeneacetic acid, 4-bromo-HCID 74654—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-bromo-phenyl)-N-heptyl-acetamideHCID 4475836—

Reaktionsschritte

A stirred solution of (4-bromo-phenyl)-acetic acid (0.186 mol, 40.0 g) and thionyl chloride (0.558 mol, 40.0 mL) in chloroform (500 mL) under a N2 atmosphere was heated under reflux for 20 hours. The mixture was cooled to room temperature and evaporated under vacuum to give an oil. This was dissolved in anhydrous methylene chloride (150 mL) and added dropwise to a solution of heptylamine (0.20 mol, 30.3 mL) and N,N-diisopropylethylamine (0.37 mol, 64.7 mL) in anhydrous methylene chloride cooled to 0° C. The mixture was stirred at room temperature for 45 minutes then poured into water and extracted with methylene chloride. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The solid residue was purified by crystallization from ethyl acetate/hexanes to give 2-(4-bromo-phenyl)-N-heptyl-acetamide as a white solid. (37 g, 64%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699904B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-25fe1573b1714939984f8e042e7152fd
Quellennotizuspto-grants-2004_03