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Diethyl Sulfate → 2-(3-Ethoxyphenyl)imidazo[2,1-a]isoquinoline

HRID 616717
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반응식

HRID 616717 반응식
[OH:1][C:2]1[CH:3]=[C:4]([C:8]2[N:9]=[C:10]3[C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH:13]=[CH:12][N:11]3[CH:20]=2)[CH:5]=[CH:6][CH:7]=1.[OH-].[K+].S(OCC)(O[CH2:27][CH3:28])(=O)=O>C(O)C>[CH2:27]([O:1][C:2]1[CH:3]=[C:4]([C:8]2[N:9]=[C:10]3[C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH:13]=[CH:12][N:11]3[CH:20]=2)[CH:5]=[CH:6][CH:7]=1)[CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6163Diethyl SulfateHCID 14797Potassium HydroxideHCID 13156070HCID 13156070, 화합물

생성물 1

HCID 131560722-(3-Ethoxyphenyl)imidazo[2,1-a]isoquinoline

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

2-(3-Hydroxyphenyl)imidazo[2,1-a]isoquinoline (2.07 g.) is added to 0.63 g. of 85 percent potassium hydroxide in 25 ml. of ethanol. To this mixture, 1.56 ml. of diethyl sulfate in 5 ml. of ethanol is added at 0° to 5° C. The mixture is maintained for 16 hours at room temperature, then is refluxed for 30 minutes. After cooling, the solution is evaporated to dryness and the residue is washed thoroughly with water. Crystallization of the solid from ethanol yields 1 g. of the title product, melting at 102°-3° C.

후처리

  1. temperatureis refluxed for 30 minutes
  2. temperatureAfter cooling
  3. customthe solution is evaporated to dryness
  4. washthe residue is washed thoroughly with water
  5. customCrystallization of the solid from ethanol
  6. customyields 1 g

출처 및 근거

ORD 기록
ord-5e3c9b1d38074db185496ccb0e33a8a9
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04075342

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