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Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde

HRID 29247
ノート
印刷プレビュー

反応式

HRID 29247 の反応式
[I:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[Cl-].[Mg+2].[Cl-].C(N(CC)CC)C.[CH2:19]=[O:20].[Cl-].[NH4+]>C(#N)C>[I:1][C:2]1[CH:7]=[CH:6][C:5]([CH:19]=[O:20])=[C:4]([OH:8])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 712FormaldehydeHCID 8471TriethylamineHCID 122723-IodophenolHCID 25517Ammonium ChlorideHCID 5360315Magnesium Chloride

生成物 1

HCID 183515132-Hydroxy-4-iodobenzaldehyde収率 160.1%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

実験手順

To a solution of 3-iodophenol (3.00 g, 13.6 mmol) in acetonitrile (50 mL) was added magnesium chloride (3.89 g, 40.9 mmol), triethylamine (7.6 mL, 55 mmol), and paraformaldehyde (1.64 g, 55 mmol). The reaction mixture was refluxed overnight, then neutralized with saturated aqueous ammonium chloride. The resultant red precipitate was removed by filtration, and the filtrate was extracted with ethyl acetate. The precipitate was dissolved in methanol and added to the combined organic extracts, which were then dried over magnesium sulfate. The solvent was removed under reduced pressure to provide an orange solid (5.4 g) as the crude product. This material was used in the subsequent step without further purification.

後処理

  1. temperatureThe reaction mixture was refluxed overnight
  2. customThe resultant red precipitate was removed by filtration
  3. extractionthe filtrate was extracted with ethyl acetate
  4. dissolutionThe precipitate was dissolved in methanol
  5. additionadded to the combined organic extracts, which
  6. dry with materialwere then dried over magnesium sulfate
  7. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-02721cc0f01345be9e12390ff0c5239e
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07420066B2

反応ノート

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