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

HRID 2220099
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인쇄 미리보기

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HRID 2220099 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-4a987e1ffdd34657b2887579273812da
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07417043B2

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