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620-80-4

620-80-4 Structure

620-80-4 Structure
IdentificationBack Directory
[Name]

2-Acetyl-3-phenylacrylic acid ethyl ester
[CAS]

620-80-4
[Synonyms]

ETHYL ALPHA-ACETYLCINNAMATE
Ethyl2-benzylideneacetoacetate
ethyl 2-benzylidene-3-oxobutanoate
α-Benzylideneacetoacetic acid ethyl
α-Acetylbenzeneacrylic acid ethyl ester
2-Acetyl-3-phenylacrylic acid ethyl ester
2-Acetyl-3-phenylpropenoic acid ethyl ester
2-Benzylidene-3-oxobutyric acid ethyl ester
2-Benzylidene-3-oxobutanoic acid ethyl ester
ethyl (2Z)-3-oxo-2-(phenylMethylidene)butanoate
3-oxo-2-(phenylmethylene)Butanoic acid ethyl ester
Butanoic acid, 3-oxo-2-(phenylmethylene)-, ethyl ester
[Molecular Formula]

C13H14O3
[MDL Number]

MFCD00731150
[MOL File]

620-80-4.mol
[Molecular Weight]

218.25
Chemical PropertiesBack Directory
[Melting point ]

60.5°C
[Boiling point ]

296°C (estimate)
[density ]

1.1367 (rough estimate)
[FEMA ]

4597 | ETHYL ALPHA-ACETYLCINNAMATE
[refractive index ]

1.5090 (estimate)
[storage temp. ]

2-8°C
[Appearance]

Light yellow to yellow Solid
[Odor]

at 100.00 %. balsamic aroma with tropical fruit notes
[Odor Type]

balsamic
[JECFA Number]

4597
[LogP]

2.21
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Acetyl-3-phenylacrylic acid ethyl ester(620-80-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl acetoacetate

141-97-9

Benzaldehyde

100-52-7

2-Acetyl-3-phenylacrylic acid ethyl ester

620-80-4

To an anhydrous DMSO solution containing L-proline (30 mol%) was added benzaldehyde (1 eq.). The reaction mixture was stirred at room temperature for 8-10 minutes, followed by the slow addition of ethyl acetoacetate (1.2 eq.) at the same temperature. The reaction system was warmed up to 80 °C with continuous stirring for 6-8 hours. Upon completion of the reaction, ethyl acetate (10 mL) was added to the mixture and stirred for several minutes before quenching the reaction with cold water. The organic and aqueous phases were separated and the aqueous phase was extracted with ethyl acetate (3 x 20 mL). The organic phases were combined, washed with saturated saline and dried with anhydrous sodium sulfate. After concentration under reduced pressure to remove the solvent, the crude product was purified by column chromatography on silica gel (60-120 mesh), the eluent being a hexane solution of 5% ethyl acetate.

[References]

[1] Chemistry - A European Journal, 2017, vol. 23, # 21, p. 4962 - 4966
[2] Dalton Transactions, 2014, vol. 43, # 9, p. 3691 - 3697
[3] Journal of the Chemical Society, Perkin Transactions 1, 1980, p. 2645 - 2656
[4] Kinetics and Catalysis, 2011, vol. 52, # 4, p. 536 - 539
[5] Research on Chemical Intermediates, 2012, vol. 38, # 1, p. 25 - 35
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