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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1527010생성일: 2026년 10월 27일

Hydrochloric Acid → tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1527010

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,4-DioxaneHCID 31275—
반응물Sodium BicarbonateHCID 516892—
반응물tert-butyl 4-((S)-1-((S)-1,1-dimethylethylsulfinamido)ethyl)piperidine-1-carboxylateHCID 117779509—
용매MethanolHCID 887—
생성물tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 22647295110.5%

반응 단계

To a 1 L round bottomed flask charged with a magnetic stir bar was added crude tert-butyl 4-((S)-1-((S)-1,1-dimethylethylsulfinamido)ethyl)piperidine-1-carboxylate (29 g) was taken up in MeOH (200 mL) before addition of a 4 N solution of HCl in 1,4-dioxane (24.06 ml, 96 mmol). The resulting solution was then stirred at room temperature for 1 h at rt. The methanol was then removed in vacuo to afford viscous oil which was treated with sat'd aqueous NaHCO3 (˜500 mL) and extracted with ethyl acetate (2×500 mL). This organic phase was combined, dried with MgSO4, filtered, and solvent was then removed in vacuo affording the title compound (22 g) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09085583B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-8eef3beea22d4af69f787986754d9d2c
출처 메모uspto-grants-2015_07