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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33697생성일: 2026년 10월 23일

4-Hydroxybenzaldehyde → 4-Piperidin-1-ylmethyl-phenol

https://huagongshe.com/ko/reaction/33697

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물PiperidineHCID 8082—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
생성물4-Piperidin-1-ylmethyl-phenolHCID 11636972—

반응 단계

A solution of 4-hydroxybenzaldehyde (10 g), piperidine (8.9 mL), and acetic acid (4.7 mL) in DCE (200 mL) was treated with sodium triacetoxyborohydride (24 g). After 16 h, the resulting mixture was treated with saturated aqueous sodium bicarbonate (100 mL) and extracted with DCM (5×100 mL). The combined organic phases were dried (magnesium sulfate) and evaporated. Trituration of the residue with ethyl acetate gave the title compound as a white crystalline solid (5.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429586B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-30552338e6264365b23655f40314d983
출처 메모uspto-grants-2008_09