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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79729생성일: 2026년 10월 24일

4-Piperidinecarboxylic acid → 1-Carbobenzoxy-4-piperidinecarboxylic Acid

https://huagongshe.com/ko/reaction/79729

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참여 물질

역할이름HCID투입량
반응물4-Piperidinecarboxylic acidHCID 3773—
반응물Benzyl chloroformateHCID 10387—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
생성물1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 73648991.2%

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온도0 °C

반응 단계

Piperidine-4-carboxylic acid (64.8 g, 0.5 mol) in H2O (50 mL) was treated with NaOH (44.0 g, 1.1 mol). The reaction mixture was cooled to 0° C. and treated with CbzCl (93.8 g, 0.55 mol). The reaction mixture was stirred at ambient temperature for 4 hours and the mixture was extracted with Et2O (3 150 mL). The aqueous phase was acidified with 6 N HCl (140 mL) and extracted with EtOAc (3 200 mL). The solution was dried over MgSO4, filtered, and concentrated to afford crude piperidine-1,4-dicarboxylic acid monobenzyl ester (120 g), which was used without further purification: MS (ESI) m/z 262 [M−H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841278B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fb9c46f13c284be7a5dbf978b5db7cdc
출처 메모uspto-grants-2014_09