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Hydrochloric Acid → 4-Iodo-2-(trifluoromethyl)phenol

HRID 403689
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HRID 403689 반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9].[OH-].[Na+].[I-:14].[Na+].Cl[O-].[Na+].Cl>CO.[Cl-].[Na+].O>[I:14][C:7]1[CH:6]=[CH:5][C:4]([OH:9])=[C:3]([C:2]([F:10])([F:11])[F:1])[CH:8]=1
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참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 14798Sodium HydroxideHCID 679582-TrifluoromethylphenolHCID 23665760Sodium Hypochlorite

생성물 1

HCID 533389294-Iodo-2-(trifluoromethyl)phenol

시약·촉매·용매 2

HCID 887
Methanol
용매
HCID 57417360Sodium chloride; water용매

실험 절차

A solution of 2-trifluoromethylphenol (10 g, 61.7 mmol) in methanol (125 mL) at room temperature was treated with sodium hydroxide (13.87 g, 93 mmol) and stirred until homogeneous. The mixture was cooled in an ice bath and sodium iodide (2.96 g, 74 mmol) was added portionwise followed by the addition of 10% sodium hypochlorite (84 mL, 136 mmol) dropwise, dividing these reagents into 3 portions and adding them sequentially over 30 minutes. The solution was then adjusted to pH 1 by dropwise addition of concentrated hydrochloric acid and poured into brine. The product was extracted into ethyl acetate, concentrated in vacuo and purified by silica gel flash chromatography eluting with ethyl acetate/hexane (0% to 5%) to give the title compound.

후처리

  1. temperatureThe mixture was cooled in an ice bath
  2. additionadding them sequentially over 30 minutes
  3. extractionThe product was extracted into ethyl acetate
  4. concentrationconcentrated in vacuo
  5. custompurified by silica gel flash chromatography
  6. washeluting with ethyl acetate/hexane (0% to 5%)

출처 및 근거

ORD 기록
ord-2139dac5196f468d956ed520d0f70cb4
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748443B2

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