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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1858565생성일: 2026년 10월 25일

Hydrochloric Acid → (3RS,4RS)-4-(4-Fluorophenyl)-3-(3-hydroxy-naphthalen-2-ylmethoxy)-piperidine

https://huagongshe.com/reaction/1858565

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물tert-butyl (3RS,4RS)-4-(4-fluorophenyl)-3-[3-(2-trimethylsilyl-ethoxy-methoxy)-naphthalen-2-ylmethoxy]-piperidine-1-carboxylateHCID 86604392—
생성물(3RS,4RS)-4-(4-Fluorophenyl)-3-(3-hydroxy-naphthalen-2-ylmethoxy)-piperidineHCID 22126512—

반응 단계

In an analogous manner to that described in Examples 3 and 5(g), by cleaving off the two protecting groups with methanolic hydrochloric acid from tert-butyl (3RS,4RS)-4-(4-fluorophenyl)-3-[3-(2-trimethylsilyl-ethoxymethoxy)-naphthalen-2-yl-methoxy]-piperidine-1-carboxylate there was obtained (3RS,4RS)-4-(4-fluorophenyl)-3-(3-hydroxy-naphthalen-2-yl-methoxy)-piperidine as a colourless solid, MS: 351 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06150526
출처 데이터셋uspto-grants-2000_11
ORD IDord-0db57ab265cd43008e0e5452598f02f6
출처 메모uspto-grants-2000_11