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4-(3-Methoxyphenyl)piperidine → 4-(3-Hydroxyphenyl)piperidine

HRID 1070727
노트
인쇄 미리보기

반응식

HRID 1070727 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1>Br>[NH:12]1[CH2:13][CH2:14][CH:9]([C:5]2[CH:4]=[C:3]([OH:2])[CH:8]=[CH:7][CH:6]=2)[CH2:10][CH2:11]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 107028904-(3-Methoxyphenyl)piperidine

생성물 1

HCID 105834534-(3-Hydroxyphenyl)piperidine

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
120 °C

실험 절차

4-(3-Methoxy-phenyl)-piperidine (1.7 g) was dissolved in 48-% HBr (60 ml) and stirred at 120° C. under an Argon-atmosphere for 3 h. The excess of HBr was then evaporated and absolute ethanol added and evaporated. This procedure was repeated several times to yield dry crystals of 3-piperidin-4-yl-phenol×HBr (2.3 g). MS m/z (relative intensity, 70 eV) 177 (M+, bp), 176 (23), 91 (14), 57 (44), 56 (60).

후처리

  1. customThe excess of HBr was then evaporated
  2. additionabsolute ethanol added
  3. customevaporated
  4. customto yield
  5. dry with materialdry crystals of 3-piperidin-4-yl-phenol×HBr (2.3 g)

출처 및 근거

ORD 기록
ord-e297217984d14d93898d33242c0f519d
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06903120B2

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