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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217506Erstellt: 24. Oktober 2026

Iodine → 1-Iodo-3-methoxy-5-(trifluoromethyl)benzene

https://huagongshe.com/de/reaction/217506

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTert-Butyl nitriteHCID 10906—
Edukt5-(Trifluoromethyl)-m-anisidineHCID 605671—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelChloroformHCID 6212—
Produkt1-Iodo-3-methoxy-5-(trifluoromethyl)benzeneHCID 19773106—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

3-methoxy-5-(trifluoromethyl)aniline (100 mg, 0.52 mmol) was dissolved in CHCl3 (5.2 mL) and t-butyl nitrite (124 μL, 1.05 mmol) was added dropwise by syringe. Iodine (266 mg, 1.05 mmol) was added and then the reaction was slowly heated to 50° C. and was maintained at this temperature for an hour and thirty minutes. The reaction was then cooled to room temperature and poured into aq. NaHSO3 (50 mL). The mixture was extracted with EtOAc (50 mL) and the organic extracts were washed with aq. NaHSO3 (3×50 mL) and brine (20 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 1% to 15% EtOAc/hexanes afforded 1-iodo-3-methoxy-5-(trifluoromethyl)benzene. Rf=0.75 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.53 (s, 1H), 7.41 (s, 1H), 7.09 (s, 1H), 3.82 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193365B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-c321e336100044fd94451ca9baf8a52b
Quellennotizuspto-grants-2012_06