Iodine → 5-Iodo-2,4-dimethylbenzoic acid

HRID 541189

反応式

HRID 541189 の反応式
[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[I:12]([O-])(=O)(=O)=O.[Na+].II.S(=O)(=O)(O)O.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(O)(=O)C.O>[I:12][C:8]1[C:9]([CH3:11])=[CH:10][C:2]([CH3:1])=[C:3]([CH:7]=1)[C:4]([OH:6])=[O:5]

参加物

8

反応物 5

HCID 807IodineHCID 1118Sulfuric AcidHCID 118972,4-Dimethylbenzoic acidHCID 24477Sodium ThiosulfateHCID 23667635Sodium periodate

生成物 1

HCID 230918755-Iodo-2,4-dimethylbenzoic acid収率 162.9%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

A solution of 2,4-dimethylbenzoic acid (20 g, 133.18 mmol, 1.00 equiv), sodium periodate (14.27 g, 66.72 mmol, 0.50 equiv), iodine (37.25 g, 146.76 mmol, 1.10 equiv), and sulfuric acid (1.96 g, 19.98 mmol, 0.15 equiv) in acetic acid (150 mL) was stirred at 110° C. in an oil bath. After 6 h, the reaction mixture was allowed to reach ambient temperature and was then diluted with 1.2 L of water. To this was carefully added 800 mL of aq Na2S2O3 (aq., sat.). The resulting solids were collected by filtration, dissolved in 1.2 L of ethyl acetate, and washed with 1×300 mL of Na2S2O3 (aq., sat.) followed by 1×400 mL of brine. The organic layer was dried (Na2SO4) and concentrated under reduced pressure. The crude residue was re-crystallized from ethanol:H2O (2:1) to yield 30 g (82%) of the title compound as a white solid.

後処理

  1. customto reach ambient temperature
  2. filtrationThe resulting solids were collected by filtration
  3. dissolutiondissolved in 1.2 L of ethyl acetate
  4. washwashed with 1×300 mL of Na2S2O3 (aq., sat.)
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. customThe crude residue was re-crystallized from ethanol:H2O (2:1)

出典と根拠

ORDレコード
ord-71925f748cbd4e50a6e93e09ecaac4a8
出典データセット
uspto-grants-2014_10
特許番号
US08871790B2

関連ノート

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