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Phenol → 1-(4-Hydroxyphenyl)-2-(4-methoxyphenyl)ethanone

HRID 1425791
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인쇄 미리보기

반응식

HRID 1425791 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([OH:12])=O)=[CH:5][CH:4]=1.[C:13]1([OH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[OH:19][C:13]1[CH:18]=[CH:17][C:16]([C:10](=[O:12])[CH2:9][C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)=[CH:15][CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 996PhenolHCID 76904-Methoxyphenylacetic Acid

생성물 1

HCID 126053601-(4-Hydroxyphenyl)-2-(4-methoxyphenyl)ethanone수율 20.6%

반응 조건

온도
80 °C

실험 절차

To a solution of 2-(4-methoxyphenyl)acetic acid (10 g, 0.06 mol) in PPA (20 mL) was added dropwise phenol (5.6 g, 0.06 mol) under an inert atmosphere. The mixture was then stirred at 80° C. for 1 h, quenched with cold water and extracted with EtOAc (2×300 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo to obtain the crude product which was purified via silica gel column chromatography to afford 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-ethanone (3 g, 20%) as a pale yellow solid

후처리

  1. customquenched with cold water
  • extractionextracted with EtOAc (2×300 mL)
  • dry with materialThe combined organic layers were dried over Na2SO4
  • concentrationconcentrated in vacuo
  • customto obtain the crude product which
  • customwas purified via silica gel column chromatography
  • 출처 및 근거

    ORD 기록
    ord-7e27769738cd4829b515b853a8390d68
    출처 데이터셋
    uspto-grants-2015_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08933074B2

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