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HRID 17864Erstellt: 23. Oktober 2026

Nipecotic Acid → 1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid

https://huagongshe.com/de/reaction/17864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNipecotic AcidHCID 4498—
EduktBenzyl chloroformateHCID 10387—
EduktSodium HydroxideHCID 14798—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—

Reaktionsschritte

To an ice cooled solution of nipecotic acid (10.0 g, 77.5 mmol), sodium hydroxide (3.4 g, 85 mmol), and tetrahydrofuran (50 mL) in water (100 mL) was added by simultaneous dropwise addition benzylchloroformate (13.3 mL, 93 mmol) in tetrahydrofuran (50 mL) and sodium hydroxide (3.4 g, 85 mmol) in water (50 mL). Warmed slowly to room temperature. After 24 hours tetrahydrofuran was removed in vacuo and the resulting aqueous mixture acidified with 3 N hydrochloric acid and extracted with dichloromethane (3×). The combined organic portions were dried with anhydrous magnesium sulfate. Filtration followed by evaporation of the filtrate in vacuo gave the titled compound. 1HNMR (CHCl3, 300 MHz) □ 7.45-7.20 (m, 5H); 5.14 (m, 2H); 4.21 (br s, 1H); 3.96 (m, 1H), 3.15 (br s, 1H); 2.93 (m, 1H); 2.51 (m, 1H); 2.09 (m, 1H); 1.80-1.60 (m, 2H); 1.50 (m, 1H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741322B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-41a63700f6cc44a0b5ecf557890effc5
Quellennotizuspto-grants-2010_06