Water → 4-(4-Ethoxyphenyl)pyridine

HRID 1617313

반응식

HRID 1617313 반응식
C(=O)([O-])[O-].[Na+].[Na+].[N:7]1[CH:12]=[CH:11][C:10](B(O)O)=[CH:9][CH:8]=1.[CH2:16]([O:18][C:19]1[CH:24]=[CH:23][C:22](I)=[CH:21][CH:20]=1)[CH3:17].O>O1CCOCC1.CO>[CH2:16]([O:18][C:19]1[CH:24]=[CH:23][C:22]([C:10]2[CH:11]=[CH:12][N:7]=[CH:8][CH:9]=2)=[CH:21][CH:20]=1)[CH3:17]

참가 물질

7

반응물 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 2207001-Ethoxy-4-iodobenzeneHCID 2734379(Pyridin-4-yl)boronic acid

생성물 1

HCID 707009334-(4-Ethoxyphenyl)pyridine

시약·촉매·용매 2

HCID 887Methanol용매HCID 312751,4-Dioxane용매

실험 절차

Under inert gas atmosphere 88 mg (0.12 mmol) PdCl2(dppf)xCH2Cl2, 13.6 mL (27.2 mmol) 2N sodium carbonate solution and 1.64 g (13.3 mmol) pyridine-4-boronic acid are added to 3.00 g (12.1 mmol) 1-ethoxy-4-iodo-benzene in 18 mL 1,4-dioxane and 6 mL methanol. The mixture is stirred for 2 d at reflux. After that time, water is added. The precipitate is filtered off, taken up in DCM and extracted with water. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; gradient DCM:MeOH 100:0→95:5) to yield the desired product which is directly used in the next reaction step.

후처리

  1. temperatureat reflux
  2. filtrationThe precipitate is filtered off
  3. extractionextracted with water
  4. dry with materialThe organic layer is dried over sodium sulphate
  5. customthe solvent is evaporated
  6. customThe residue is purified by column chromatography (silica gel; gradient DCM:MeOH 100:0→95:5)

출처 및 근거

ORD 기록
ord-71ae10d6a4d24a50bd57f81488ef55cf
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08765959B2

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