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Diethyl Ether → 5-Bromo-2-ethylpyridine

HRID 850118
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HRID 850118 반응식
[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]
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참가 물질

7

반응물 3

HCID 3283Diethyl EtherHCID 693532,5-DibromopyridineHCID 178418443HCID 178418443, 화합물

생성물 1

HCID 139797365-Bromo-2-ethylpyridine수율 76%

시약·촉매·용매 3

HCID 3007855Zincchloride촉매HCID 11979704
Tetrakis(triphenylphosphine)palladium
촉매
HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-6066826c41484cc78574173cd1051802
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06015825

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