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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446221Erstellt: 24. Oktober 2026

Methyl iodide → Methyl 3-iodo-4-methyl-5-nitrobenzoate

https://huagongshe.com/de/reaction/446221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt3-Iodo-4-methyl-5-nitrobenzoic acidHCID 59627777—
LösungsmittelAcetoneHCID 180—
ProduktMethyl 3-iodo-4-methyl-5-nitrobenzoateHCID 2472811098,3%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of 3-iodo-4-methyl-5-nitro-benzoic acid (16.06 g, 52.3 mmol) in acetone (300 mL) was added K2CO3 (14.46 g, 104.6 mmol) followed by methyl iodide ((3.91 mL, 62.76 mmol). The reaction mixture was stirred at 40° C. overnight, then cooled to room temperature and partitioned between ethyl acetate and brine. The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure to provide 16.5 g (98%) of 3-iodo-4-methyl-5-nitro-benzoic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476457B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-846b869706134fd28e8d18aa2de0e38b
Quellennotizuspto-grants-2013_07