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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323055Erstellt: 23. Oktober 2026

Triethylamine → N-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)urea

https://huagongshe.com/de/reaction/323055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt1,3-Dioxaindane-4-carboxylic acidHCID 304832—
Edukt2-Amino-5-NitrophenolHCID 4984721—
LösungsmittelTolueneHCID 1140—
ProduktN-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)ureaHCID 988343242%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of the 2,3-methylenedioxyphenylcarboxylic acid in toluene, triethylamine (0.27 mL, 1.95 mmol) and diphenylphosphoryl azide (DPPA) (0.32, mL, 1.5 mmol) were added. The reaction mixture was stirred at 60° C. for 2 hours, then 2-amino-5-nitrophenol (250 mg, 1.5 mmol) was added. The reaction mixture was stirred at 100° C. for 18 hours. After the reaction mixture was cooled to room temperature, it was partitioned between 5% citric acid and ethyl acetate. The organic layer was separated and the aqueous layer was extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography of the resulting solid on silica gel (hexane:ethyl acetate; 5:1) gave product (200 mg, 42%). EI-MS m/z 318 (M+H)+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211373B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-ef0995265c31454f9a3e3ffc16bdabb9
Quellennotizuspto-grants-2001_04