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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 470642Erstellt: 24. Oktober 2026

3',4'-Dimethoxycinnamic acid → HCID 67398066, Verbindung

https://huagongshe.com/de/reaction/470642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3',4'-Dimethoxycinnamic acidHCID 16848—
EduktN'-hydroxynonanimidamideHCID 5074022—
LösungsmittelTolueneHCID 1140—
ProduktHCID 67398066HCID 67398066—

Reaktionsschritte

To a solution of 0.59 g (2.84 mmol) of 3-(3,4-dimethoxy-phenyl)-acrylic acid (compound of Example 2; Step 1) in 6 mL of toluene, 0.503 g (3.1 mmol) of 1,1-carbonyldiimidazole was added in portions at 25° C. to 30° C. under inert atmosphere. To the thickened mixture, 5 mL of toluene was added and the resulting mixture was stirred at 25° C. to 30° C. for 60 to 90 min. A solution of N-hydroxynonanimidamide (compound of example 47; 1.0 g, 3.8 mmol) diluted with 5 mL of toluene was added to the above reaction mixture at 25° C. to 30° C. The reaction mixture was stirred at 25° C. to 30° C. under nitrogen for 12-14 h, followed by stirring at 100° C. to 105° C. for 6-8 h. After completion of the reaction, the reaction mixture was cooled to 25° C. to 30° C. and quenched with 10 mL of chilled water under stirring at 25° C. to 30° C. The organic layer was separated, and the aqueous layer was washed with 5 mL of toluene. The organic layers were combined and washed with 10 mL of 1N HCl solution, 10 mL of 5% sodium bicarbonate solution and 10 mL of 10% sodium chloride solution. The organic layer was distilled to obtain a crude residue, which was purified by column chromatography (silica gel, chloroform-methanol) to yield the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629277B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-9f4b5b65f8c2421eafca406fd3dd39ac
Quellennotizuspto-grants-2014_01