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Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde

HRID 29247
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HRID 29247 반응식
[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
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참가 물질

7

반응물 5

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

생성물 1

HCID 183515132-Hydroxy-4-iodobenzaldehyde수율 160.1%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-02721cc0f01345be9e12390ff0c5239e
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07420066B2

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