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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29749생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidine

https://huagongshe.com/ko/reaction/29749

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물[1-(tert-Butoxycarbonyl)piperidin-4-yl]acetic acidHCID 1512539—
반응물DiboronHCID 6328200—
반응물HCID 178418361HCID 178418361—
용매TetrahydrofuranHCID 8028—
생성물1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 85414097%

반응 단계

To a solution of 4-carboxymethyl-piperidine-1-carboxylic acid tert-butyl ester (16.7 g, 69.0 mmol) in THF (100 mL) was added diborane (151 mL, 1.0 M solution in THF) over a period of 10 min at 0° C. Hydrogen gas was rapidly evolved and after gas evolution had ceased the reaction was stirred at room temperature for 1 h. The reaction mixture was again cooled to 0° C., and 1 M aqueous HCl was added dropwise to the reaction mixture with further evolution of hydrogen. Addition of HCl was continued until the evolution of hydrogen had almost ceased. The mixture was then stirred for 10 min and made basic (pH 13-14) by the addition of 1 M NaOH solution. The aqueous solution was extracted with ethyl acetate, the organic phase washed with brine, dried and concentrated under reduced pressure to yield 4-(2-hydroxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester (15.2 g, 97%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423012B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-870351fe873143bfacb4192cca891f8c
출처 메모uspto-grants-2008_09