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Iodine → 2-Fluoro-6-iodo-4-methylaniline

HRID 400599
ノート
印刷プレビュー

反応式

HRID 400599 の反応式
[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH2:9].[I:10]I>CO.OO>[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([I:10])[C:3]=1[NH2:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 807IodineHCID 679842-Fluoro-4-methylaniline

生成物 1

HCID 109779002-Fluoro-6-iodo-4-methylaniline収率 87.6%

試薬・触媒・溶媒 2

HCID 784Hydrogen Peroxide溶媒HCID 887Methanol溶媒2 回

実験手順

A solution of 2-fluoro-4-methylphenylamine (1.25 g, 10 mmol) in 5 mL of methanol was treated with a solution of iodine (1.27 g, 5 mmol) in a mixture of 25 mL of methanol and 3 mL of hydrogen peroxide over a period of 15 minutes at room temperature. After 18 hours, the reaction mixture was quenched with 30 mL of saturated aqueous sodium thiosulfate and extracted with three 50 mL portions of dichloromethane. The combined organic layers were washed with two 30 mL portions of saturated sodium bisulfite solution, three 50 mL portions of water, dried over sodium sulfate, and concentrated in vacuo. Chromatography on SiO2 (10% ethyl acetate in hexanes) gave 1.1 g of the title product as a light brownish oil (44% yield).

後処理

  1. customthe reaction mixture was quenched with 30 mL of saturated aqueous sodium thiosulfate
  2. extractionextracted with three 50 mL portions of dichloromethane
  3. washThe combined organic layers were washed with two 30 mL portions of saturated sodium bisulfite solution, three 50 mL portions of water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-f2188e324455469d907cc77fb48a578e
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08741897B2

反応ノート

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