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Iodine → 4-Chloro-5-iodo-2-methylbenzoic acid

HRID 541294
ノート
印刷プレビュー

反応式

HRID 541294 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[CH:3]=1.[I:12]I.S(=O)(=O)(O)O>C(O)(=O)C>[Cl:1][C:2]1[C:10]([I:12])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 807IodineHCID 1118Sulfuric AcidHCID 3482694-Chloro-2-methylbenzoic acid

生成物 1

HCID 682889484-Chloro-5-iodo-2-methylbenzoic acid

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
110 °C

実験手順

To a round-bottom flask was added a solution of 4-chloro-2-methylbenzoic acid (30.0 g, 176 mmol, 1.00 equiv) in acetic acid (300 mL). NaIO4 (19.0 g, 88.8 mmol, 0.50 equiv), I2 (49.0 g, 193 mmol, 1.10 equiv), and sulfuric acid (3 mL) were added to the reaction. The resulting mixture was stirred overnight at 110° C. After cooling to ambient temperature, the reaction was carefully quenched with 500 mL of Na2S2O3 (aq., sat.). The resulting solids were collected by filtration and then dissolved in 500 mL of ethyl acetate. The organic phase was washed with 2×200 mL of brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. This resulted in 20.0 g (38%) of 4-chloro-5-iodo-2-methylbenzoic acid as a white solid.

後処理

  1. temperatureAfter cooling to ambient temperature
  2. customthe reaction was carefully quenched with 500 mL of Na2S2O3 (aq., sat.)
  3. filtrationThe resulting solids were collected by filtration
  4. dissolutiondissolved in 500 mL of ethyl acetate
  5. washThe organic phase was washed with 2×200 mL of brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThis resulted in 20.0 g (38%) of 4-chloro-5-iodo-2-methylbenzoic acid as a white solid

出典と根拠

ORDレコード
ord-6accd657c61143f78d8345e0113e9818
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871790B2

反応ノート

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