Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1473863Erstellt: 25. Oktober 2026

4-Piperidinecarboxylic acid → 1-(3-Bromo-5-cyanophenyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1473863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Piperidinecarboxylic acidHCID 3773—
EduktTriethylamineHCID 8471—
EduktDimethylacetamideHCID 31374—
Edukt3-Bromo-5-fluorobenzonitrileHCID 2783330—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(3-Bromo-5-cyanophenyl)piperidine-4-carboxylic acidHCID 59588189—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A mixture of 3-bromo-5-fluorobenzonitrile (1.6 g, 7.8 mmol), piperidine-4-carboxylic acid (2.6 g, 12.0 mmol), triethylamine (4.0 mL, 28.5 mmol) and N,N-dimethylacetamide (1.5 mL) in a sealed tube was heated to 130° C. for 48 hr. The reaction mixture was diluted with EtOAc and water. The organic layer was separated, dried (MgSO4), and concentrated to give a crude reside which was purified by chromatography on silica gel (CH2Cl2/MeOH) to afford 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09018205B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-d29d1020a44143528ce1a4ffac2d4325
Quellennotizuspto-grants-2015_04