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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Coumaric acid → 4-Vinylphenol

HRID 327751
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HRID 327751 반응식
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7]C(O)=O)=[CH:4][CH:3]=1.C1(C=CC(O)=CC=1)O.N12CCCN=C1CCCCC2>CS(C)=O>[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3224-Coumaric acidHCID 785HydroquinoneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

생성물 1

HCID 624534-Vinylphenol

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
135 °C

실험 절차

In a 1-liter sulfonating flask equipped with mechanical stirrer, reflux condenser and nitrogen delivery line, 300 ml of dimethyl sulfoxide are added to 150 g (0.91 mol) of 4-hydroxycinnamic acid, 6 g (54 mmol) of hydroquinone and 6 g (39 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene. The mixture is then heated at 135° C. for 31/2 hours. After cooling, the mixture is poured onto ice and extracted three times with 500 ml of diethyl ether, and the organic phase is washed five times with 100 ml of water, dried over magnesium sulfate and concentrated. The resulting oil is recrystallised twice from n-hexane to yield 69.07 g (0.58 mol, 63% of the theoretical yield) of 4-hydroxystyrene in the form of a white powder (m.p. 68° C.).

후처리

  1. customequipped with mechanical stirrer
  2. temperaturereflux condenser
  3. temperatureAfter cooling
  4. additionthe mixture is poured onto ice
  5. extractionextracted three times with 500 ml of diethyl ether
  6. washthe organic phase is washed five times with 100 ml of water
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. customThe resulting oil is recrystallised twice from n-hexane
  10. customto yield 69.07 g (0.58 mol, 63% of the

출처 및 근거

ORD 기록
ord-dee086b3dbe7405ca4cdb115ec555481
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05274060

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