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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14291Erstellt: 23. Oktober 2026

Hydrochloric Acid → 3-Iodo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/de/reaction/14291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium IodideHCID 4875—
Edukt3-Amino-5-(methoxycarbonyl)benzoic acidHCID 13557643—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
Produkt3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 1584039155,1%

Reaktionsschritte

To an ice-cold, stirred solution of 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in a 2 N hydrochloric acid (156 mL) was added a solution of sodium nitrite (1.84 g, 26.67 mmol) in water (10.8 mL). This mixture was then added dropwise to an ice-cold, stirred solution of potassium iodide (8.84 g, 53.25 mmol) in water (26.2 mL). After stirring for 35 min, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium thiosulfate, and saturated sodium chloride, dried (sodium sulfate), and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50:50:2 hexanes/ethyl acetate/acetic acid) afforded 3-iodo-5-(methoxycarbonyl)benzoic acid (4.48 g): 1H NMR (500 MHz, DMSO-d6): δ 13.49 (br s, 1H), 8.45-8.38 (m, 3H), 3.83 (s, 3H); ESI-MS (m/z): 305 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b9e365e738df4d5f94ed7d7af91e7e2d
Quellennotizuspto-grants-2010_06