Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 732259Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/de/reaction/732259

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanolHCID 16067438—
Edukt[(4'-Bromo-1,1'-biphenyl-4-yl)oxy]-valeric acidHCID 68986501—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN,N'-DicyclohexylureaHCID 4277—

Reaktionsschritte

3.26 g of a mixture of 80% of EDT-methanol and 20% of hydroxy-PDT (corresponding to 18.9 mmol; 15.1 mmol based on the main component EDT-methanol), 3.14 g (15.2 mmol) of N,N′-dicyclohexylcarbodiimide and 0.3 g (2.45 mmol) of 4-(dimethylamino)pyridine are dissolved in 100 ml of CH2Cl2 and cooled in an ice bath. 5.25 g (15.0 mmol) of [(4′-bromo-1,1′-biphenyl-4-yl)oxy]-valeric acid are added a spatula at a time to the ice-cooled solution while stirring. After 1 hour, the reaction is continued at room temperature. After a further 65 hours, the colourless precipitate formed (N,N′-dicyclohexylurea) is filtered off. The clear, colourless solution is washed in succession with 3×250 ml of 1 N HCl, 3×150 ml of saturated NaHCO3 solution and 1×150 ml and 2×100 ml of saturated NaCl solution. The organic phase is dried over MgSO4, the desiccant is filtered off and the solvent is removed on a rotary evaporator. This gives 7.98 g of crude product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585983B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-93dc93d0dcec4b96afcb99d02f908758
Quellennotizuspto-grants-2009_09