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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1649578Erstellt: 26. Oktober 2026

Acetic Anhydride → 2,2'-[[2-[(3-Iodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic acid

https://huagongshe.com/reaction/1649578

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktNitrilotriacetic AcidHCID 8758—
Edukt3-Iodo-p-toluidineHCID 118889—
LösungsmittelPyridineHCID 1049—
Produkt2,2'-[[2-[(3-Iodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic acidHCID 1324524856,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A slurry of 4.78 g of nitrilotriacetic acid in 40 ml of dry pyridine (dried over molecular sieves) is heated to 60° C. Acetic anhydride (2.55 g) is added slowly and the solution is heated to 100° C. After heating for 0.5 hour, the solution is cooled to 40° C. and a solution of 5.8 g of 3-iodo-4-methylaniline in 20 ml of dry pyridine is added over 25 minutes. The solution is heated at 100° C. for 1.0 hour. The reaction is cooled and rotary evaporated to a residue which is dissolved in 65 ml of 10% sodium hydroxide. This solution is extracted twice with 50 ml portions of methylene chloride diluted with 100 ml of distilled water, and neutralized with concentrated HCl to pH 3.2. The crude product is refrigerated for about 16 hours, filtered, washed twice with 50 ml portions of distilled water, and dried under vacuum at 40° C. The crude product (8.0 g) is recrystallized after Darco treatment to yield 5.7 g of product, melting point 213.5°-215.0° C. (dec).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04418208
Quelldatensatzuspto-grants-1983_11
ORD IDord-62d6e1441a1249ac9a5107a72e8e43ae
Quellennotizuspto-grants-1983_11