Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40591Erstellt: 24. Oktober 2026

Cyclohexanol → 4-(4-Cyclohexyloxy-benzyl)-piperazine-1-carboxylic acid phenylamide

https://huagongshe.com/de/reaction/40591

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexanolHCID 7966—
EduktTriphenylphosphineHCID 11776—
EduktDi-tert-butyl azodicarboxylateHCID 97268—
Edukt4-(4-Hydroxy-benzyl)-piperazine-1-carboxylic acid phenylamideHCID 57880877—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4-Cyclohexyloxy-benzyl)-piperazine-1-carboxylic acid phenylamideHCID 1156026528%

Reaktionsschritte

To a mixture of 4-(4-hydroxy-benzyl)-piperazine-1-carboxylic acid phenylamide (311 mg) and cyclohexanol (150 mg) in DCM (4 mL) was added polymer-supported Ph3P (500 mg) followed by di-tert-butyl azodicarboxylate (345 mg). The reaction mixture was shaken overnight, and filtered. Chromatography of the filtrate gave the title compound as a white solid (110 mg). 1H NMR (400 MHz, CDCl3): 7.36-7.19 (m, 6H), 7.05-7.00 (m, 1H), 6.88-6.84 (m, 2H), 6.30 (s, 1H), 4.25-4.20 (m, 1H), 3.50-3.47 (m, 6H), 2.48-2.46 (m, 4H), 2.01-1.97 (m, 2H), 1.82-1.80 (m, 2H), 1.60-1.29 (m, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530476B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-da542b1dd56f49ae9b0c0d75241f7941
Quellennotizuspto-grants-2013_09