Water → methyl (E)-3-(2-methoxy-5-pyrimidinyl)acrylate

HRID 1378968Notes

Reaction equation

HRID 1378968 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6](I)=[CH:5][N:4]=1.C(=O)([O-])[O-].[K+].[K+].[C:16]([O:20][CH3:21])(=[O:19])[CH:17]=[CH2:18].O>CN(C)C=O.[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6](/[CH:18]=[CH:17]/[C:16]([O:20][CH3:21])=[O:19])=[CH:5][N:4]=1

Participants

8

Conditions

Temperature
80 °C

Procedure

2-Methoxy-5-iodopyrimidine (1.736 g, 7.36 mmol) was dissolved in 36 ml of N,N-dimethylformamide, and 99 mg of palladium acetate, 2.54 g (18.4 mmol) of potassium carbonate, 2.05 g (7.36 mmol) of tetrabutylammonium chloride and 3.168 g (36.8 mmol) of methyl acrylate were added thereto. The mixture was stirred in an argon atmosphere at 80° C. for 1 hour. Water was added to the reaction mixture, and the solution was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The obtained crude product was purified by silica-gel column chromatography (250 ml of silica gel, hexane:ethyl acetate=2:1 to 1:1) to give 1.26 g (6.49 mmol) of methyl (E)-3-(2-methoxy-5-pyrimidinyl)acrylate (yield: 88%).

Workup

  1. extractionthe solution was extracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained crude product
  6. customwas purified by silica-gel column chromatography (250 ml of silica gel, hexane:ethyl acetate=2:1 to 1:1)

Sources & evidence

ORD record
ord-2476fc2cca2a458ca728c4b80882b3c2
Source dataset
uspto-grants-1997_09
Patent number
US05670492

Reaction notes

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