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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30470생성일: 2026년 10월 24일

Piperidine → 3-Bromo-5-(piperidin-1-ylmethyl)pyridine

https://huagongshe.com/ko/reaction/30470

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
생성물3-Bromo-5-(piperidin-1-ylmethyl)pyridineHCID 6718880571%

반응 단계

5-Bromo-pyridine-3-carbaldehyde (0.190g, 1 mmol), NaB(OAc)3H (0.320 g, 1.50 mmol) and piperidine (0.090 g, 1.05 mmol) were suspended in DCM (8 mL) and the reaction mixture was stirred overnight at rt. The reaction was quenched by the addition of 1 M NaOH solution (5 mL) and the mixture was stirred for 1 h. The reaction mixture was extracted with DCM (3×15 mL). The organic extracts were combined, dried over Na2SO4, filtered, and concentrated to yield a crude oily product (0.18 g, 71%). This crude product was carried to the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423147B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f27ee76980884117baec2023d5ba8948
출처 메모uspto-grants-2008_09