Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2964Erstellt: 23. Oktober 2026

P-Anisidine → 2-bromo-N-(4-methoxyphenyl)acetamide

https://huagongshe.com/de/reaction/2964

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-AnisidineHCID 7732—
EduktBromoacetyl bromideHCID 61147—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-bromo-N-(4-methoxyphenyl)acetamideHCID 532213—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

The title compound was prepared via a modification of the literature procedure (Vloon, W. J.; Kruk, C.; Pandit, U. K.; Hofs, H. P.; McVie, J. G. J. Med Chem. 1987, 30, 20-4.). To a solution of 4-methoxyaniline (4.93 g, 40.0 mmol) in methylene chloride (200 mL) was added diisopropylethylamine (7.66 mL, 44.0 mmol). The resulting mixture was cooled to -20° C., and bromoacetyl bromide (3.82 mL, 44.0 mmol) was added slowly. The reaction mixture was warmed to room temperature over 20 minutes and stirred additional 30 minutes. The reaction mixture was diluted with water (100 mL), stirred for 30 minutes and the organic layer was separated. The organic layer was washed with water (2×100 mL), brine (100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (9.68 g) which was recrystallized from ethyl acetate to provide bromo-N-(4'-methoxyphenyl)acetamide as a whim crystal (6.31 g, 65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731438
Quelldatensatzuspto-grants-1998_03
ORD IDord-a73c3e09e44447508491ea934b7c975c
Quellennotizuspto-grants-1998_03