Hydrogen Peroxide → 3-(2-Hydroxyethyl)-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one

HRID 391731

反応式

HRID 391731 の反応式
C12BC(CCC1)CCC2.[CH3:10][O:11][C:12]1[CH:17]=[C:16]([N+:18]([O-:20])=[O:19])[CH:15]=[CH:14][C:13]=1[N:21]1[CH:26]=[CH:25][CH:24]=[C:23]([CH:27]=[CH2:28])[C:22]1=[O:29].[OH-].[Na+].OO.S(OS([O-])=O)([O-])=[O:35].[Na+].[Na+]>O1CCCC1>[OH:35][CH2:28][CH2:27][C:23]1[C:22](=[O:29])[N:21]([C:13]2[CH:14]=[CH:15][C:16]([N+:18]([O-:20])=[O:19])=[CH:17][C:12]=2[O:11][CH3:10])[CH:26]=[CH:25][CH:24]=1

参加物

7

反応物 5

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 24346Disodium disulfiteHCID 789669-Borabicyclo(3.3.1)nonaneHCID 594101761-(2-Methoxy-4-nitrophenyl)-3-vinylpyridin-2(1H)-one

生成物 1

HCID 594101813-(2-Hydroxyethyl)-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

At 0° C., a solution of 36 g (299 mmol) of 9-borabicyclo[3.3.1]nonane in 600 ml of tetrahydrofuran is added over a period of 45 min to 37 g (136 mmol) of the compound from Example 20A. After a further hour at this temperature, a solution of 27 g (680 mmol) of sodium hydroxide (1N in water) is added over the course of 15 min. The mixture is stirred for a further 5 min, and 125 ml of a 30% strength hydrogen peroxide solution are then added such that the temperature does not exceed 30° C. Cooling is removed, and the mixture is stirred for another 30 min. The mixture is extracted repeatedly with ethyl acetate, the combined organic phases are washed with a solution of 730 g (1.50 mol) of sodium disulphite, the organic phase is separated off and the aqueous phase is reextracted with ethyl acetate. The combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulphate and evaporated to dryness under reduced pressure. The residue is absorbed on silica gel and chromatographed using a gradient of cyclohexane and ethyl acetate. The product fractions are combined and evaporated to dryness under reduced pressure. For crystallization, tert-butyl methyl ether is added. The crystals are filtered off and dried under reduced pressure. This gives 24 g (60% of theory) of the desired product.

後処理

  1. waitAfter a further hour at this temperature
  2. customdoes not exceed 30° C
  3. temperatureCooling
  4. customis removed
  5. stirringthe mixture is stirred for another 30 min
  6. extractionThe mixture is extracted repeatedly with ethyl acetate
  7. customthe organic phase is separated off
  8. washThe combined organic phases are washed with saturated sodium chloride solution
  9. dry with materialdried over magnesium sulphate
  10. customevaporated to dryness under reduced pressure
  11. customThe residue is absorbed on silica gel
  12. customchromatographed
  13. customevaporated to dryness under reduced pressure
  14. customFor crystallization, tert-butyl methyl ether
  15. additionis added
  16. filtrationThe crystals are filtered off
  17. customdried under reduced pressure

出典と根拠

ORDレコード
ord-8bdd8a5f210448cfa0039004cbc375fa
出典データセット
uspto-grants-2013_02
特許番号
US08383822B2

関連ノート

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