Hydrochloric Acid → 4-Chloro-1-(pyridin-3-YL)butan-1-one

HRID 1534360Notes

Reaction equation

HRID 1534360 reaction equation
[C:1]([O:9]C)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.[CH2:11]1[CH2:16]OC(=O)[CH2:12]1.C[O-].[Na+].[ClH:20].C(=O)(O)[O-].[Na+]>O1CCOCC1>[Cl:20][CH2:12][CH2:11][CH2:16][C:1]([C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1)=[O:9]

Participants

7

Reactant 5

HCID 313Hydrochloric AcidHCID 7151Methyl NicotinateHCID 7302Gamma-ButyrolactoneHCID 516892Sodium BicarbonateHCID 10942334Sodium Methoxide

Product 1

HCID 124710054-Chloro-1-(pyridin-3-YL)butan-1-one

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

A solution of methyl nicotinate (59 g, 0.43 mol), 4-hydroxybutyric acid lactone (51.8 g, 0.602 mol), and sodium methoxide (70 g, 1.29 mol) in dioxane (500 mL) is refluxed for 1 hour and then cooled. Concentrated hydrochloric acid (650 mL) is added, and the reaction mixture refluxed for 12 hours. The resulting solution is neutralized with solid sodium bicarbonate and extracted with chloroform. The organic phase is dried (sodium sulfate), and the solvent evaporated in vacuo. The residue is taken up in 2-propanol (50 mL) and treated with a saturated solution of hydrogen chloride in 2-propanol. The hydrochloride salt of 4-chloro-1-(3-pyridinyl)-1-butanone is obtained as a white solid (30 g); mp 73-76° C.

Workup

  1. temperaturecooled
  2. temperaturethe reaction mixture refluxed for 12 hours
  3. extractionextracted with chloroform
  4. dry with materialThe organic phase is dried (sodium sulfate)
  5. customthe solvent evaporated in vacuo
  6. additiontreated with a saturated solution of hydrogen chloride in 2-propanol

Sources & evidence

ORD record
ord-a67f00b8fb5140c38d751224d10563ae
Source dataset
uspto-grants-1992_02
Patent number
US05089497

Reaction notes

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