돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29754생성일: 2026년 10월 24일

Hydrochloric Acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/29754

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
반응물DiboronHCID 6328200—
반응물HCID 178418361HCID 178418361—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081100.2%

반응 단계

To a solution of piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (19.3 g, 84.0 mmol) in THF (100 mL) was added diborane (185 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-Hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (18.12 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423012B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-91d40b688a9b498cabf1e210a690dcf9
출처 메모uspto-grants-2008_09