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HRID 17864생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Nipecotic AcidHCID 4498—
반응물Benzyl chloroformateHCID 10387—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741322B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-41a63700f6cc44a0b5ecf557890effc5
출처 메모uspto-grants-2010_06