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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23958생성일: 2026년 10월 24일

1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/23958

반응식

참여 물질

역할이름HCID투입량
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
반응물Borane;tetrahydrofuranHCID 2723981—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408185%

반응 조건

온도0 °C

반응 단계

1-Boc-isonipecotic acid (10.0 g, 214 mmol) was dissolved in THF (400 mL) and cooled to 0° C. A solution of BH3-THF (180 mL, 1 N in THF, 180 mmol) was added slowly. The mixture stirred for 1 h at 0° C. and was allowed to warm to room temperature for 12 h. The mixture was carefully quenched with water and diluted with ethyl acetate. The water layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried (Na2SO4), filtered and concentrated to provide l-Boc-piperidine-4-methanol (7.98 g, 85%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855715B1
출처 데이터셋uspto-grants-2005_02
ORD IDord-69907c3ae526490195aad8c034f65fdb
출처 메모uspto-grants-2005_02