Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44166Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → 4-Carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)propanoate

https://huagongshe.com/de/reaction/44166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-HydroxybenzamideHCID 65052—
EduktNaproxenHCID 156391—
EduktHCID 178418300HCID 178418300—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)propanoateHCID 5934559332%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To the solution of 1 (naproxen, 4 g, 17.4 mmol) in 80 mL of dimethylformamide, hydroxybenzotriazole (2.59 g, 19.14 mmol) and DCC (2.59 g, 19.14 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 3.58 g, 26.1 mmol) was added and stirred for 1 h at 0° C. and 2 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, with NaHCO3 5%, with citric acid 10% and than dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9.5/0.5), from which 4-carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)-propanoate (5) was obtained (1.91 g, 32% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541398B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-bf5b7215cf1a4ccc83d7a4850936d780
Quellennotizuspto-grants-2013_09