Allyl bromide → HCID 86594466、化合物

HRID 1408494ノート

反応式

HRID 1408494 の反応式
[F:1][C:2]([F:22])([C:12]([F:21])([F:20])[C:13]([F:19])([F:18])[C:14]([F:17])([F:16])[F:15])[CH2:3][CH2:4][SiH:5]([CH:9]([CH3:11])[CH3:10])[CH:6]([CH3:8])[CH3:7].C([Br:26])C=C>Cl[Pd]Cl>[F:22][C:2]([F:1])([C:12]([F:20])([F:21])[C:13]([F:18])([F:19])[C:14]([F:15])([F:16])[F:17])[CH2:3][CH2:4][Si:5]([Br:26])([CH:9]([CH3:11])[CH3:10])[CH:6]([CH3:8])[CH3:7]

参加物

4

反応物 2

HCID 7841Allyl bromideHCID 16211428Diisopropyl(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane

生成物 1

HCID 86594466HCID 86594466、化合物

試薬・触媒・溶媒 1

HCID 24290Palladium Chloride触媒

反応条件

温度
60 °C

実験手順

In an oven-dried round-bottom flask equipped with a stir bar and cooled under N2, 3,3,4,4,5,5,6,6,6-nonafluorohexyldiisopropylsilane (10.1 g, 27.8 mmol) was dissolved in allyl bromide (20 mL), and PdCl2 (50 mg) was added. The solution was heated to 60° C. for 15 hr, then cooled, and concentrated via rotary evaporation. The resulting suspension was dissolved in pentane, filtered to remove residual catalyst, and then solvent was removed to yield (3,3,4,4,5,5,6,6,6-nonafluorohexyldiisopropylsilyl)bromide (12.1 g) as a pale brown liquid. The bromide was treated under anhydrous conditions with 1.2 eq. (based on initial silane) of ethynylmagnesium bromide and heated to 40° C. for 6 hr. The reaction was quenched with water and dilute sulfuric acid, pentane was added, and the organic layer was separated. The organic layer was washed with water (6×50 mL), dried over MgSO4, filtered, and concentrated via rotary evaporation. Further purification via flash chromatography using hexane yielded pure (3,3,4,4,5,5,6,6,6-nonafluorohexyldiisopropylsilyl)acetylene (9.90 g, 25.6 mmol, 92%) as a colorless liquid. Analysis of the product provided the following data: 1H-NMR (200 MHz, CDCl3) δ=2.4 (s, 1H), 2.2 (m, 2H), 1.1 (m, 14H), 0.8 (m, 2H).

後処理

  1. customIn an oven-dried round-bottom flask equipped with a stir bar
  2. temperaturecooled under N2
  3. temperaturecooled
  4. concentrationconcentrated via rotary evaporation
  5. dissolutionThe resulting suspension was dissolved in pentane
  6. filtrationfiltered
  7. customto remove residual catalyst
  8. customsolvent was removed

出典と根拠

ORDレコード
ord-c4cbff989ef24c2ab4a450b58fef29a4
出典データセット
uspto-grants-2014_12
特許番号
US08920679B2

反応ノート

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