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Diethyl Ether → 5-Bromo-2-ethylpyridine

HRID 850118
ノート
印刷プレビュー

反応式

HRID 850118 の反応式
[CH2:1]([Mg]Br)[CH3:2].CCOCC.Br[C:11]1[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][N:12]=1>C1COCC1.[Cl-].[Zn+2].[Cl-].[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH2:1]([C:11]1[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][N:12]=1)[CH3:2]
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 3

HCID 3283Diethyl EtherHCID 693532,5-DibromopyridineHCID 178418443HCID 178418443、化合物

生成物 1

HCID 139797365-Bromo-2-ethylpyridine収率 76%

試薬・触媒・溶媒 3

HCID 3007855Zincchloride触媒HCID 11979704Tetrakis(triphenylphosphine)palladium
触媒
HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

A solution of ethylmagnesium bromide in ether (100 ml, 3M, 0.3 mol) was added dropwise to a cold (5° C.) solution of anhydrous zinc chloride (40.9 g, 0.3 mol) in THF (500 ml) under nitrogen. After stirring for one hour at 0° C., tetrakis(triphenylphosphine)-palladium (0) (1.0 g, 0.87 mmol) was added followed by a solution of 2,5-dibromopyridine (50 g, 0.21 mol) in THF (200 ml). The resulting yellow suspension was stirred at room temperature overnight, quenched by the addition of water (200 ml) and then evaporated in vacuo. The residue was treated with a suspension of ethylenediaminetetraacetic acid (200 g) in water (1000 ml) and dichloromethane (500 ml). The organic layer was separated and the aqueous layer again extracted with dichloromethane (500 ml). The combined extracts were dried (MgSO4), solvent evaporated in vacuo, and the residue distilled (123-124° C., 60 mmHg) to give the required product as a colourless oil (28.8 g, 76%).

後処理

  1. stirringThe resulting yellow suspension was stirred at room temperature overnight
  2. customquenched by the addition of water (200 ml)
  3. customevaporated in vacuo
  4. additionThe residue was treated with a suspension of ethylenediaminetetraacetic acid (200 g) in water (1000 ml) and dichloromethane (500 ml)
  5. customThe organic layer was separated
  6. extractionthe aqueous layer again extracted with dichloromethane (500 ml)
  7. dry with materialThe combined extracts were dried (MgSO4), solvent
  8. customevaporated in vacuo
  9. distillationthe residue distilled (123-124° C., 60 mmHg)

出典と根拠

ORDレコード
ord-6066826c41484cc78574173cd1051802
出典データセット
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06015825

反応ノート

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