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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481602생성일: 2026년 10월 25일

Methanol → (2s)-(-)-1-(4-Indolyloxy)-3-(4-phenoxypiperidin-1-yl)-2-propanol ethanedioate

https://huagongshe.com/reaction/481602

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Oxalic AcidHCID 971—
반응물4-PhenoxypiperidineHCID 18878—
반응물(2s)-Glycidyl indol-4-yl etherHCID 10943254—
용매Ethyl AcetateHCID 8857—
생성물(2s)-(-)-1-(4-Indolyloxy)-3-(4-phenoxypiperidin-1-yl)-2-propanol ethanedioateHCID 131719687—

반응 단계

The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 4-(phenoxy)piperidine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 69% overall yield. FDMS m/e=366 (M+ of free base). α[D]589 =-14.29 (c=0.5, methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789402
출처 데이터셋uspto-grants-1998_08
ORD IDord-6e934172234940b59a65106d36e98ad6
출처 메모uspto-grants-1998_08