Pyridine → t-Butyl isobutyrylacetate

HRID 1532793Notes

Reaction equation

HRID 1532793 reaction equation
[CH3:1][C:2]1([CH3:10])[O:9][C:7](=[O:8])[CH2:6][C:4](=[O:5])O1.N1C=C[CH:14]=[CH:13][CH:12]=1.[C:17](Cl)(=O)C(C)C>C(Cl)Cl>[CH3:12][CH:13]([CH3:14])[C:4](=[O:5])[CH2:6][C:7]([O:9][C:2]([CH3:1])([CH3:10])[CH3:17])=[O:8]

Participants

5

Conditions

Temperature
0 °C

Procedure

Meldrum's acid (80 g, 555 mmol) was dissolved in 600 mL of CH2Cl2 and cooled to 0° C. Freshly distilled pyridine (87.8 g, 1.11 mol) was added to the CH2Cl2 solution and then isobutyryl chloride (65.0 g, 610.5 mmol) was added to the mixture via a pressure equalizing addition funnel. The reaction was stirred at 0° C. for 1 hr and then warmed to rt and stirred for 2 hr. Then, the reaction was quenched with water (200 mL) and washed with 0.5 M HCl (×2), water (×1), and brine (×1). The organize layer was dried over MgSO4 and concentrated in vacuo. The crude product was azeotropically dried with benzene (250 mL), and then dissolved in 200 mL of benzene and 200 mL of tert-butanol was added. The resultant reaction was heated at reflux for 4 hr. After this period, the volatiles were removed in vacuo and the product then distilled on the high vacuum pump (bp 62-63° C., 0.1 mm Hg). The desired β-keto ester 1E was obtained (58.6 g, 315.5 mmol) in 57% yield as a clear, colorless, light oil.

Workup

  1. additionaddition funnel
  2. temperaturewarmed to rt
  3. stirringstirred for 2 hr
  4. customThen, the reaction was quenched with water (200 mL)
  5. washwashed with 0.5 M HCl (×2), water (×1), and brine (×1)
  6. dry with materialThe organize layer was dried over MgSO4
  7. concentrationconcentrated in vacuo
  8. dry with materialThe crude product was azeotropically dried with benzene (250 mL)
  9. dissolutiondissolved in 200 mL of benzene
  10. addition200 mL of tert-butanol was added
  11. customThe resultant reaction
  12. temperaturewas heated
  13. temperatureat reflux for 4 hr
  14. waitAfter this period
  15. customthe volatiles were removed in vacuo
  16. distillationthe product then distilled on the high vacuum pump (bp 62-63° C., 0.1 mm Hg)

Sources & evidence

ORD record
ord-8f303a2c65c343a0a2e72fcf647f8073
Source dataset
uspto-grants-2001_03
Patent number
US06204388B1

Reaction notes

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