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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17865Erstellt: 24. Oktober 2026

Oxalyl chloride → benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/de/reaction/17865

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produktbenzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylateHCID 2776575—

Reaktionsschritte

To an ice cooled methylene chloride solution of 1-[(Benzyloxy)carbonyl]piperidine-3-carboxylic acid (512 mg, 1.95 mmol) under nitrogen was added oxalyl chloride (0.185 mL, 1.95 mmol) and a few drops N,N-dimethylformamide. The reaction flask was warmed slowly to room temperature and after 2 hours the solvent was removed in vacuo. Toluene was added and removed in vacuo (2×) to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741322B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-41058c22e6b04ecb9835b0c445873296
Quellennotizuspto-grants-2010_06