홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Undecafluoropiperidine → 2-Fluoropyridine

HRID 483884
노트
인쇄 미리보기

반응식

HRID 483884 반응식
[F:1][C:2]1(F)[C:7](F)(F)[C:6](F)(F)[C:5](F)(F)[C:4](F)(F)[N:3]1F>F>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:2]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 136658Undecafluoropiperidine

생성물 2

HCID 1049Pyridine수율 8%HCID 97462-Fluoropyridine수율 13%

시약·촉매·용매 1

HCID 14917Hydrofluoric Acid용매

실험 절차

Recently attentiaon has been directed to the use of compounds of the N-F class, i.e. having an N-F bond, as electrophilic fluorinating agents. The prototypical member of this class is perfluoro-N-fluoropiperidine (R. E. Banks and G. E. Williamson, Chem. Ind. (London), 1964, 1864 and R. E. Banks et al, J. Chem. Soc., Perkin Trans. I, 1972, 1098). However, this compound is obtainable only in low yields by electrochemical fluorination of pyridine (about 8% yield) or 2-fluoropyridine (about 13% yield) in anhydrous hydrogen fluoride. Furthermore, it has been found to be inadequately reactive in several applications and, on transfer of fluorine to a carbanionic substrate, liberates the imidoyl fluoride perfluoro-1-azacyclohex-1-ene which then competes for the substrate. Similar problems militate against use of the analogous compounds perfluoro-(N-fluoro-2,6-dimethylpiperidine) and perfluoro-N-fluoromorpholine (R. E. Banks et al, J. Chem. Soc., Perkin Trans. I, 1988, 2805) and of poly[perfluoro-(N-fluoropiperidin-4-ylethylene)] (R. E. Banks & E. Tsiliopoulos, J. Fluorine Chem., 1986, 34, 281) as electrophilic fluorinating agents.

출처 및 근거

ORD 기록
ord-fd3cc9f3155d4393b7df585862d225be
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05227493

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트