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Potassium Iodide → (4-Iodophenylethynyl)trimethylsilane

HRID 2262329
ノート
印刷プレビュー

反応式

HRID 2262329 の反応式
[CH3:1][Si:2]([C:5]#[C:6][C:7]1[CH:13]=[CH:12][C:10](N)=[CH:9][CH:8]=1)([CH3:4])[CH3:3].N([O-])=O.[Na+].[I-:18].[K+]>Cl>[CH3:1][Si:2]([C:5]#[C:6][C:7]1[CH:13]=[CH:12][C:10]([I:18])=[CH:9][CH:8]=1)([CH3:4])[CH3:3]
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 3

HCID 4875Potassium IodideHCID 110524294-[(Trimethylsilyl)ethynyl]anilineHCID 23668193Sodium Nitrite

生成物 1

HCID 11808725(4-Iodophenylethynyl)trimethylsilane収率 92%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

As shown in the following Reaction 2, 250 mg (1.32 mmol) of 4-trimethylsilylethynylaniline obtained in A of Example 1-1 was melted in 3 mL of hydrochloric acid at the temperature of 0° C., and 94 mg (1.37 mmol, 1.04 eq) of sodium nitrite was added thereto, and then the reaction solution was stirred for 1 hour. After completion of stirring, 280 mg (1.69 mmol, 1.28 eq) of potassium iodide was added to the reaction solution, and then the reaction solution was stirred at room temperature for 12 hours. Next, the reaction solution was extracted with ether 2 times and 1 time with 1M sodium chloride aqueous solutions 1 time. The organic solvent layer was dehydrated with magnesium sulfate, filtered, and then distilled under reduced pressure. The compound distilled under reduced pressure was purified with an alumina column chromatography (mobile phase: hexane) to obtain 360 mg of 4-trimethylsilylethynyl iodobenzene with the yield of 92%. NMR data of the obtained compound is as follows. [1H NMR (400 MHz, CDCl3): δ 0.23-0.27 (m, 9H), 7.16 (d, 2H), 7.69 (d, 2H)].

後処理

  1. customobtained in A of Example 1-1
  2. additionwas added
  3. stirringAfter completion of stirring
  4. stirringthe reaction solution was stirred at room temperature for 12 hours
  5. extractionNext, the reaction solution was extracted with ether 2 times and 1 time with 1M sodium chloride aqueous solutions 1 time
  6. filtrationfiltered
  7. distillationdistilled under reduced pressure
  8. distillationThe compound distilled under reduced pressure
  9. customwas purified with an alumina column chromatography (mobile phase: hexane)

出典と根拠

ORDレコード
ord-3b967c2ef80a4622b227c53c6895959b
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07850872B2

反応ノート

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