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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Potassium Carbonate → HCID 21270184, 화합물

HRID 1194473
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HRID 1194473 반응식
[OH:1][C:2]1[CH:19]=[CH:18][C:5]2[C:6](=[O:17])[C:7]([C:10]3[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=3)=[CH:8][O:9][C:4]=2[C:3]=1O.[C:21](=[O:24])([O-])[O-].[K+].[K+].S([O-])(O[CH3:31])(=O)=O>CC(C)=O>[CH3:31][O:1][C:2]1[CH:19]=[CH:18][C:5]2[C:6](=[O:17])[C:7]([C:10]3[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=3)=[CH:8][O:9][C:4]=2[C:3]=1[O:24][CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 4694097Methyl sulfate(1-)HCID 5481241HCID 5481241, 화합물

생성물 1

HCID 21270184HCID 21270184, 화합물

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

7,8-Dihydroxy-3-(4-methylphenyl)-4H-1-benzopyran-4-one (2.7 g), described in example 9, is dissolved in dry acetone (50 ml). Pyrolyzed potassium carbonate (4.14 g) is added and the mixture is heated to reflux. A solution of methyl sulphate (3.78 g) in acetone (10 ml) is then added dropwise and heating is maintained for three more hours. After cooling, the solid is filtered and the solution is evaporated to dryness under vacuum. Water is added to the residue which is filtered, washed with an aqueous sodium hydroxide solution (1N) then with water and dried. After crystallization in methanol, 7,8-dimethoxy-3-(4-methylphenyl)-4H-1-benzopyran-4-one is obtained, m.p. 135°.

후처리

  1. temperaturethe mixture is heated to reflux
  2. temperatureheating
  3. temperatureis maintained for three more hours
  4. temperatureAfter cooling
  5. filtrationthe solid is filtered
  6. customthe solution is evaporated to dryness under vacuum
  7. additionWater is added to the residue which
  8. filtrationis filtered
  9. washwashed with an aqueous sodium hydroxide solution (1N)
  10. dry with materialwith water and dried
  11. customAfter crystallization in methanol

출처 및 근거

ORD 기록
ord-2b5b1880c66d49e893a283b139f4345a
출처 데이터셋
uspto-grants-1989_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04814346

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