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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384324Erstellt: 26. Oktober 2026

Methyl iodide → 1-Bromo-2-methoxy-5-methyl-3-nitrobenzene

https://huagongshe.com/reaction/384324

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-4-methyl-6-nitrophenolHCID 29918—
LösungsmittelAcetoneHCID 180—
Produkt1-Bromo-2-methoxy-5-methyl-3-nitrobenzeneHCID 1386018397,9%

Reaktionsschritte

2-Bromo-4-methyl-6-nitro-phenol 11b (22.24 g, 95.9 mmol) was dissolved in 150 mL of acetone, followed by addition of potassium carbonate (15.9 g, 115 mmol) and iodomethane (13.7 mL, 220.6 mmol). The reaction mixture was heated to reflux overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was diluted with 100 mL of ethyl acetate and filtered. The mixture was concentrated under reduced pressure to obtain the title compound 1-bromo-2-methoxy-5-methyl-3-nitro-benzene 11c (23.1 g, yield 97.9%) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367710B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-143aadf36a0342eeb5c2baaea9543ba4
Quellennotizuspto-grants-2013_02