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Methyl Isobutyl Ketone → 2-Isopropyl-4-nitrophenol

HRID 502628
ノート
印刷プレビュー

反応式

HRID 502628 の反応式
[CH3:1][CH:2]([CH3:7])[CH2:3][C:4](=[O:6])[CH3:5].O.[N+:9]([CH:12]([CH:15]=O)[CH:13]=O)([O-:11])=[O:10].[Na].[OH-].[Na+]>C(O)C.O>[CH:2]([C:3]1[CH:15]=[C:12]([N+:9]([O-:11])=[O:10])[CH:13]=[CH:5][C:4]=1[OH:6])([CH3:7])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 7909Methyl Isobutyl KetoneHCID 14798Sodium HydroxideHCID 71317419Sodium nitromalonaldehyde hydrate

生成物 1

HCID 5289542-Isopropyl-4-nitrophenol収率 54%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

4-Methyl-2-pentanone (4.85 g, 48 mmol) in 40 mL of ethanol was added dropwise to a solution of sodium nitromalonaldehyde monohydrate (7.61 g, 48 mmol) in 40 mL of water. NaOH (48 ml of 1N aqueous solution) was then added to the reaction mixture. The mixture was stirred at room temperature overnight, and solvent was removed under reduced pressure. The residue was diluted with water and neutralized, then extracted with ethyl acetate. The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was purified by column chromatography with silica eluting with 15% ethyl acetate in hexanes to yield 4.7 g of 2-isopropyl-4-nitrophenol.

後処理

  1. customsolvent was removed under reduced pressure
  2. additionThe residue was diluted with water
  3. extractionneutralized, then extracted with ethyl acetate
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified by column chromatography with silica eluting with 15% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-4e7713e699974148b743aef39dfc210a
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07776872B2

反応ノート

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