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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 489573Erstellt: 25. Oktober 2026

Iodine → Methyl 5-chloro-4-iodo-2-methoxybenzoate

https://huagongshe.com/reaction/489573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktSulfuric AcidHCID 1118—
EduktPotassium IodideHCID 4875—
EduktMethyl 4-amino-5-chloro-2-methoxybenzoateHCID 700493—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
ProduktMethyl 5-chloro-4-iodo-2-methoxybenzoateHCID 6931479584,2%

Reaktionsbedingungen

Temperatur-1 °C

Reaktionsschritte

4-Amino-5-chloro-2-methoxy benzoic acid methyl ester of Step A (5.00 g, 23.2 mmol) was suspended in water (52 mL) and concentrated sulfuric acid (13 mL) was added. The resulting suspension was cooled to −1° C. and a solution of sodium nitrite (1.76 g, 25.5 mmol) in water (10 mL) was added at a rate which maintained the temperature below 0° C., resulting in the formation of a clear yellow solution. A mixture of potassium iodide (4.23 g, 25.5 mmol) and iodine (3.24 g, 12.8 mmol) in water (50 mL) was then added dropwise and the reaction stirred at 0° C. for 1.5 hours. The reaction mixture was warmed to room temperature and extracted with ethyl acetate. The combined extracts were washed sequentially with 1 M aqueous sodium thiosulfate, 1 N sodium hydroxide and brine, and dried over anhydrous magnesium sulfate, filtered and concentrated, whereupon the product crystallized. The resulting orange crystals were suspended in petroleum ether, filtered and dried in vacuo to provide the title compound (6.38 g), m.p. 72-73° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06977254B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-679438fc1c774f5e9fad7e4bdaabe23f
Quellennotizuspto-grants-2005_12