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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17864Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNipecotic AcidHCID 4498—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741322B2
Source datasetuspto-grants-2010_06
ORD IDord-41a63700f6cc44a0b5ecf557890effc5
Source noteuspto-grants-2010_06