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Iodine → p-(Chlorodimethylsilyl)styrene

HRID 622327
ノート
印刷プレビュー

反応式

HRID 622327 の反応式
Cl[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Mg].II.[Cl:13][Si:14](Cl)([CH3:16])[CH3:15]>O1CCCC1.C(OCC)C>[Cl:13][Si:14]([CH3:16])([CH3:15])[C:7]1[CH:8]=[CH:9][C:4]([CH:3]=[CH2:2])=[CH:5][CH:6]=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

7

反応物 4

HCID 807IodineHCID 6398DichlorodimethylsilaneHCID 12142Benzene, chloroethenyl-2 回HCID 5462224Magnesium

生成物 1

HCID 11138053p-(Chlorodimethylsilyl)styrene収率 55%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
65 °C

実験手順

Two milliliters of chlorostyrene was added to 0.97 gram of magnesium turnings in 20 milliliters (ml) of dry tetrahydrofuran under argon. A crystal, about 5 milligrams of iodine, was then added, and the reaction mixture was heated at 65° C. with an air gun until the reaction started (approximately 15 minutes). Thereafter, an additional 2.33 milliliters of chlorostyrene was added slowly to the reaction mixture with a syringe over a period of 15 minutes. The reaction mixture was then refluxed for about 5 minutes at 67° C., and then allowed to cool to room temperature. Dichlorodimethylsilane (9.7 milliliters) was then carefully added with a syringe, (the reaction was exothermic) followed by stirring at 60° C. in an oil bath for 30 minutes. The reaction mixture was then cooled to room temperature, diluted with anhydrous diethylether (approximately 75 ml), and filtered to remove the insoluble magnesium salts. Subsequently, the solvent tetrahydrofuran was removed under reduced pressure and the resulting oil was distilled to yield 3.9 grams (55 percent) of the above product, which was characterized by NMR.

後処理

  1. custom(approximately 15 minutes)
  2. temperatureThe reaction mixture was then refluxed for about 5 minutes at 67° C.
  3. temperatureto cool to room temperature
  4. temperatureThe reaction mixture was then cooled to room temperature
  5. filtrationfiltered
  6. customto remove the insoluble magnesium salts
  7. customSubsequently, the solvent tetrahydrofuran was removed under reduced pressure
  8. distillationthe resulting oil was distilled

出典と根拠

ORDレコード
ord-4dacf41190fd4aa883ae695a753cdca7
出典データセット
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04770968

反応ノート

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