Diethyl Malonate → Diethyl 2-(2-phenyl-2-propylpentanoyl)malonate

HRID 494438Notes

Reaction equation

HRID 494438 reaction equation
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[Cl-].[Mg+2].[Cl-].C(N(CC)CC)C.[C:22]1([C:28]([CH2:35][CH2:36][CH3:37])([CH2:32][CH2:33][CH3:34])[C:29](Cl)=[O:30])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C(#N)C>[C:22]1([C:28]([CH2:35][CH2:36][CH3:37])([CH2:32][CH2:33][CH3:34])[C:29]([CH:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:1]([O:9][CH2:10][CH3:11])=[O:8])=[O:30])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

A solution of diethyl malonate (3.03 g, 18.77 mmol) and anhydrous magnesium chloride in acetonitrile (36 mL) at 0° C. was treated with triethylamine (5.2 mL, 37.55 mmol), stirred at 0° C. for 30 min, stirred at 25° C. for 3 hours, cooled to 0° C. and treated dropwise with a solution of the product of Example 1D (18.77 mmol) in acetonitrile (15 mL) over 10 min and stirred at 50° C. for 18 hours. The solution was cooled to 25° C. and concentrated in vacuo. The solids were suspended in ethyl acetate and cooled to 0° C., treated with 4N HCl solution until all solids had dissolved. The organic layer was extracted with water (2×) and with saturated sodium chloride solution, dried (Na2SO4), filtered and concentrated in vacuo to afford the title compound (4.51 g, 66%). 1H NMR (300 MHz, CDCl3): δ 7.32 (m, 5 H), 4.50 (s, 1 H), 4.04 (q, J=7.35 Hz, 4 H), 1.97 (m, 4 H), 1.28 (m, 3 H), 0.98 (m, 10 H).

Workup

  1. stirringstirred at 25° C. for 3 hours
  2. temperaturecooled to 0° C.
  3. stirringstirred at 50° C. for 18 hours
  4. temperatureThe solution was cooled to 25° C.
  5. concentrationconcentrated in vacuo
  6. temperaturecooled to 0° C.
  7. additiontreated with 4N HCl solution until all solids
  8. dissolutionhad dissolved
  9. extractionThe organic layer was extracted with water (2×) and with saturated sodium chloride solution
  10. dry with materialdried (Na2SO4)
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-1233f819af2a46c8869cd5790fdce6f3
Source dataset
uspto-grants-2009_05
Patent number
US07538105B2

Reaction notes

Loading…