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p-Toluenesulfonic acid → Ethyl 2-(4-phenoxyphenyl)acetate

HRID 993078
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인쇄 미리보기

반응식

HRID 993078 반응식
[O:1]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([OH:17])=[O:16])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:18]1(C)C=CC(S(O)(=O)=O)=C[CH:19]=1>C(O)C>[O:1]([C:8]1[CH:9]=[CH:10][C:11]([CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:12][CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 2390774-Phenoxyphenylacetic acid

생성물 1

HCID 13567666Ethyl 2-(4-phenoxyphenyl)acetate수율 404.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a suspension of (4′-phenoxyphenyl)acetic acid (0.456 g) in 4 ml of ethanol is added para-toluensulfonic acid (0.076 g) and the resulting mixture is refluxed for 2 hours. The solvent is evaporated off, the residue is dissolved in diethyl ether and the organic phase is washed with saturated aqueous solution of sodium hydrogencarbonate and then with brine. The organic phase is dried over sodium sulfate and concentrated to dryness to give 0.458 g of the product as a brown oil.

후처리

  1. temperaturethe resulting mixture is refluxed for 2 hours
  2. customThe solvent is evaporated off
  3. dissolutionthe residue is dissolved in diethyl ether
  4. washthe organic phase is washed with saturated aqueous solution of sodium hydrogencarbonate
  5. dry with materialThe organic phase is dried over sodium sulfate
  6. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-9aa64fa48516403c9996634f5814ee5f
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06472396B1

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