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

HRID 403689
ノート
印刷プレビュー

反応式

HRID 403689 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

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

生成物 1

HCID 533389294-Iodo-2-(trifluoromethyl)phenol

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
HCID 57417360Sodium chloride; water溶媒

実験手順

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.

後処理

  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%)

出典と根拠

ORDレコード
ord-2139dac5196f468d956ed520d0f70cb4
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08748443B2

反応ノート

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