Triethylamine → N-(3-Methacrylamidopropyl)-3-oxobutanamide

HRID 2058312Notes

Reaction equation

HRID 2058312 reaction equation
C(N(CC)CC)C.Cl.[NH2:9][CH2:10][CH2:11][CH2:12][NH:13][C:14](=[O:18])[C:15]([CH3:17])=[CH2:16].[CH2:19]=[C:20]1[O:24][C:22](=[O:23])[CH2:21]1>CO>[C:22]([NH:9][CH2:10][CH2:11][CH2:12][NH:13][C:14](=[O:18])[C:15]([CH3:17])=[CH2:16])(=[O:23])[CH2:21][C:20]([CH3:19])=[O:24]

Participants

5

Conditions

Temperature
0 °C

Procedure

Triethylamine (24 g, 0.24 mole) was added dropwise at 0° C. to a solution of N-(3-aminopropyl)-methacrylamide hydrochloride (40 g, 0.24 mole) and diketene (20 g, 0.24 mole) in methanol (800 ml). After addition, the temperature was maintained at 0° C. for 2 hours under stirring. Stirring was continued at 20° C. for 20 hours. The solvent was then removed. The residue was dissolved in chloroform (1 liter), washed with 5% hydrochloric acid (200 ml), washed with saturated NaHCO3 (200 ml), dried over anhydrous magnesium sulfate, and filtered. Excess solvent was removed. The residue was recrystallized from benzene (500 ml) and ethyl ether (500 ml) to give N-(3-acetoacetamidopropyl)methacrylamide (m.p.=93°-94° C.) at a yield of 50%.

Workup

  1. additionAfter addition
  2. stirringStirring
  3. customThe solvent was then removed
  4. dissolutionThe residue was dissolved in chloroform (1 liter)
  5. washwashed with 5% hydrochloric acid (200 ml)
  6. washwashed with saturated NaHCO3 (200 ml)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customExcess solvent was removed
  10. customThe residue was recrystallized from benzene (500 ml) and ethyl ether (500 ml)

Sources & evidence

ORD record
ord-b49ffea2a1d0432184cc7a31ecbe5337
Source dataset
uspto-grants-1980_07
Patent number
US04215195

Reaction notes

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