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Nitric Acid → 5-Hydroxy-2-methyl-4-nitrobenzonitrile

HRID 1968979
ノート
印刷プレビュー

反応式

HRID 1968979 の反応式
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:10])=[C:6]([CH:9]=1)[C:7]#[N:8].[N+:11]([O-])([OH:13])=[O:12].O>C(Cl)Cl>[OH:1][C:2]1[C:3]([N+:11]([O-:13])=[O:12])=[CH:4][C:5]([CH3:10])=[C:6]([CH:9]=1)[C:7]#[N:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 944Nitric AcidHCID 962WaterHCID 594440865-Hydroxy-2-methylbenzonitrile

生成物 1

HCID 594441745-Hydroxy-2-methyl-4-nitrobenzonitrile収率 29.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

5-Hydroxy-2-methylbenzonitrile (D90, 475 mg, 3.57 mmol) was dissolved in DCM (5 mL) and 70% nitric acid (1 mL, 22 mmol) was added dropwise to the reaction. The mixture was stirred for 45 min before the addition of H2O (15 mL). The two phases were separated and the aqueous phase was extracted with DCM (2×). The combined organics were dried (Na2SO4) and concentrated by rotary evaporation to give a yellow solid. The crude residues were purified by flash column chromatography (silica, 10% EtOAc/90% iso-hexane to 50% EtOAc/50% iso-hexane) to give 5-hydroxy-2-methyl-4-nitrobenzonitrile (D91, 186 mg, 26%) as a yellow solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe two phases were separated
  2. extractionthe aqueous phase was extracted with DCM (2×)
  3. dry with materialThe combined organics were dried (Na2SO4)
  4. concentrationconcentrated by rotary evaporation
  5. customto give a yellow solid
  6. customThe crude residues were purified by flash column chromatography (silica, 10% EtOAc/90% iso-hexane to 50% EtOAc/50% iso-hexane)

出典と根拠

ORDレコード
ord-f6ee7599085a43ceaa15b45a747096eb
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08426443B2

反応ノート

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