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Potassium Carbonate → 1-Ethyl-3-ethynylbenzene

HRID 2240980
ノート
印刷プレビュー

反応式

HRID 2240980 の反応式
[CH2:1]([C:3]1[CH:4]=[C:5]([C:9]#[C:10][Si](C)(C)C)[CH:6]=[CH:7][CH:8]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+]>CO>[CH2:9]([C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([C:1]#[CH:2])[CH:4]=1)[CH3:10]
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

4

反応物 2

HCID 11430Potassium CarbonateHCID 67539193HCID 67539193、化合物

生成物 1

HCID 133018331-Ethyl-3-ethynylbenzene収率 110%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
25 °C

実験手順

In a 100 mL round-bottomed flask was placed ((3-ethylphenyl)ethynyl)trimethylsilane (3.17 g, 15.66 mmol) and MeOH (31.3 ml) was added to give a yellow solution. Potassium carbonate (21.65 g, 157 mmol) was added and reaction stirred at 25° C. for 1 h. The reaction was partitioned between water (200 mL) and hexanes (200 mL). The organic was washed with water (100 mL) and brine (100 mL). The organic was dried over Na2SO4. The solvent was removed providing 1-ethyl-3-ethynylbenzene (2.24 g, 17.21 mmol, 110% yield) as a dark brown oil that was used as is without further purification.

後処理

  1. customIn a 100 mL round-bottomed flask was placed
  2. customto give a yellow solution
  3. customreaction
  4. customThe reaction was partitioned between water (200 mL) and hexanes (200 mL)
  5. washThe organic was washed with water (100 mL) and brine (100 mL)
  6. dry with materialThe organic was dried over Na2SO4
  7. customThe solvent was removed

出典と根拠

ORDレコード
ord-780c1fb33ccd4ad8861e454496d62424
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723368B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート