Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238694Erstellt: 25. Oktober 2026

Methyl iodide → 1-Bromo-2-methoxy-3-nitrobenzene

https://huagongshe.com/reaction/238694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-6-nitrophenolHCID 13545453—
LösungsmittelAcetoneHCID 180—
Produkt1-Bromo-2-methoxy-3-nitrobenzeneHCID 2250571390%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2-Bromo-6-nitro-phenol 1b (46.55 g, 0.214 mol) was dissolved in 500 mL of acetone followed by addition of potassium carbonate (35.36 g, 0.26 mol) and iodomethane (20.1 mL, 0.32 mol). The reaction mixture was heated to reflux at 70° C. for 40 hours. The reaction mixture was concentrated under reduced pressure and diluted with 1300 mL of ethyl acetate and 500 mL of water. The aqueous layer was extracted with ethyl acetate (300 mL×2). The combined organic extracts were washed with 4 M hydrochloric acid and saturated sodium bicarbonate solution and then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 1-bromo-2-methoxy-3-nitro-benzene 1c (44.59 g, yield 90.0%) as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642637B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3434ac2eae604bb697f4e67b8310a985
Quellennotizuspto-grants-2014_02