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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1255774생성일: 2026년 10월 26일

Potassium Hydroxide → 4-[3-(4-Chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1255774

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매TetrahydrofuranHCID 8028—
생성물4-[3-(4-Chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 6741354175%

반응 단계

A solution of piperazine-1-carboxylic acid tert-butyl ester (19.6 g, 105 mmol) and 3-(4-chloro-phenoxy)-benzaldehyde (24.4 g, 105 mmol) in THF (90 mL) was treated with NaB(OAc)3H (33.4 g, 158 mmol). After 3 h, the resulting mixture was treated with 10% aq. KOH (500 mL). The aqueous phase was extracted with EtOAc (2×500 mL) then saturated aqueous NaCl (200 mL). The organic extracts were combined, dried (MgSO4) and purified (FCC) to give 4-[3-(4-chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester (29.6 g, 75%). MS (ESI+): calcd for C22H27ClN2O3 m/z 402.17. found 403.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461159B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-bc062b3c02614b9fa219df479bfe9aae
출처 메모uspto-grants-2013_06