Propanal → (Z)-Methyl 3-methyl-4-oxobut-2-enoate

HRID 1657211Notes

Reaction equation

HRID 1657211 reaction equation
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=O.[CH:7](=[O:10])[CH2:8][CH3:9].C(OC(=O)C)(=O)C>C1CCCCC1.N(CC(O)=O)C>[CH:7](/[C:8](/[CH3:9])=[CH:2]\[C:1]([O:5][CH3:6])=[O:4])=[O:10]

Participants

6

Procedure

18 g (0.2 mol) of sarcosine were suspended by stirring in 500 ml of cyclohexane in a flask and, starting at 20° C., a mixture of 1809 g (20.6 mol) of methyl glyoxylate and 1194 g (20.6 mol) of propionaldehyde was added within 90 min. During the dropwise addition the temperature rose slowly to the boiling point (75° C.). After the addition was complete, initially a small amount of water was removed as azeotrope, and then the mixture was distilled until the bottom temperature was 100° C. to remove cyclohexane. Then 2220 g (21.8 mol) of acetic anhydride were added to the residue, and the reaction mixture was distilled to a bottom temperature of 150° C. to remove acetic acid. Fractional distillation of the bottom product yielded 1822 g (14.2 mol) of methyl 3-formylcrotonate, corresponding to a yield of 69% of theory, with a trans/cis isomer ratio of 93/7.

Workup

  1. customstarting at 20° C.
  2. additionwas added within 90 min
  3. additionDuring the dropwise addition the temperature
  4. customrose slowly to the boiling point (75° C.)
  5. additionAfter the addition
  6. custominitially a small amount of water was removed as azeotrope
  7. distillationthe mixture was distilled until the bottom temperature
  8. customwas 100° C.
  9. customto remove cyclohexane
  10. distillationthe reaction mixture was distilled to a bottom temperature of 150° C.
  11. customto remove acetic acid
  12. distillationFractional distillation of the bottom product

Sources & evidence

ORD record
ord-61c05b7e282d4e49840ec256fd8c234c
Source dataset
uspto-grants-1993_10
Patent number
US05256813

Reaction notes

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