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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 642109Erstellt: 25. Oktober 2026

4-Methylmorpholine → Methyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoate

https://huagongshe.com/reaction/642109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktMethyl 4-aminobenzoateHCID 12082—
EduktIsobutyl chloroformateHCID 62365—
Edukt3-(Benzodioxol-5-yl)propionic acidHCID 64810—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoateHCID 994524462%

Reaktionsschritte

To a solution of 3-(3,4-methylenedioxyphenyl)-propionic acid (501 mg, 2.58 mmol) in anhydrous THF (10 mL) were added N-methylmorpholine (0.28 mL, 2.58 mmol) and isobutylchloroformate (0.33 mL, 2.58 mmol) at 0° C. After 30 min, at 0° C., a solution of methyl 4-aminobenzoate (390 mg, 2.58 mmol) in anhydrous THF (2 mL) was added to the reaction mixture. After 30 min the temperature was allowed to warm up to rt and stir for 24 hrs. After extraction with EtOAc (100 mL), washing with HCl (0.1N, 50 mL) and a saturated aqueous solution of NaHCO3 (50 mL), the organic layer was dryed over sodium sulfate and evaporated under vacuo to give a solid. The residue was taken up in Et2O, filtrated and washed with Et2O gave the title compound as a white solid (62%) in a 99.4% purity by HPLC (MaxPlot detection between 230 and 400 nm).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696231B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-4fab7c1510124c2ab47740be364e6664
Quellennotizuspto-grants-2010_04