Propionic Acid → Ethyl 2-methyl-3,4-pentadienoate
Reaction equation
C(=O)(O)[O-].[Na+].[C:6](O)(=[O:9])[CH2:7]C.C[C:12]1[CH:17]=[C:16]([C:18](C)(C)C)[C:15]([OH:22])=C(C(C)(C)C)[CH:13]=1>>[CH2:6]([O:9][C:15](=[O:22])[CH:16]([CH3:18])[CH:17]=[C:12]=[CH2:13])[CH3:7]Participants
Conditions
- Temperature
- 150 °C
Procedure
The autoclave is closed and the reaction mass is heated to 150° C. over a period of 50 minutes. The reaction mass is then maintained at a temperature of between 135°-160° C and at a pressure of 20 up to 60 psig for a period of 3 hours. At the end of this 3-hour period, the autoclave is cooled to room temperature and then opened. 12.6 g of sodium bicarbonate is then added to the reaction mass in order to neutralize the propionic acid. 30 g of Primol (see note 1) and 0.1 g of Ionol (see note 2) are added and the resulting reaction product is fractionally distilled at atmospheric pressure to a pot temperature of 129° C. A mixture of ethanol and ethyl propionate is distilled over. Vacuum is then applied to the distillation column and the resultant product, ethyl-2-methyl-3,4-pentadienoate is distilled at a vapor temperature of 65°-69° C at a pressure of 24-33 mm Hg as fractions 5-10 of the following fractions:
Workup
- customThe autoclave is closed
- temperatureThe reaction mass is then maintained at a temperature of between 135°-160° C and at a pressure of 20 up to 60 psig for a period of 3 hours
- temperatureAt the end of this 3-hour period, the autoclave is cooled to room temperature
- customthe resulting reaction product
- distillationis fractionally distilled at atmospheric pressure to a pot temperature of 129° C
- additionA mixture of ethanol and ethyl propionate
- distillationis distilled over
- distillationVacuum is then applied to the distillation column
- distillationthe resultant product, ethyl-2-methyl-3,4-pentadienoate is distilled at a vapor temperature of 65°-69° C at a pressure of 24-33 mm Hg as fractions 5-10 of the following fractions
Sources & evidence
- ORD record
- ord-e4eeca0ab198497a9fd713a67d842e5d
- Source dataset
- uspto-grants-1976_12
- Patent number
- US03998873
Reaction notes
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