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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59800Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/59800

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
PatentnummerUS09440956B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-821743cb204d42a1a8a745aa8aed2a07
Quellennotizuspto-grants-2016_09