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Ethyl 2-oxo-4-phenylbutyrate

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Ethyl 2-oxo-4-phenylbutyrate Basic information

Product Name:
Ethyl 2-oxo-4-phenylbutyrate
Synonyms:
  • 4-PHENYL-2-OXOBUTYRIC ACID ETHYL ESTER
  • 2-OXO-4-PHENYLBUTANOIC ACID ETHYL ESTER
  • 2-OXO-4-PHENYLBUTYRIC ACID ETHYL ESTER
  • BENZYLPYRUVIC ACID ETHYL ESTER
  • KETO ESTER
  • ETHYL BENZYLPYRUVATE
  • ETHYL-2 OXO-4 PHENYL BUTANOATE
  • ETHYL 2-OXO-4-PHENYLBUTYRATE
CAS:
64920-29-2
MF:
C12H14O3
MW:
206.24
EINECS:
265-276-9
Product Categories:
  • C12 to C63
  • Carbonyl Compounds
  • Intermediates of Sertraline
  • Pharmaceutical Intermediates
  • Aromatics
  • Esters
  • (intermediate of lisinopril )
  • Building Blocks
  • C12 to C63
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • 1
Mol File:
64920-29-2.mol
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Ethyl 2-oxo-4-phenylbutyrate Chemical Properties

Boiling point:
132 °C/2 mmHg (lit.)
Density 
1.091 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.504(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Oil
color 
Colourless
BRN 
2725083
CAS DataBase Reference
64920-29-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
23-24/25-36/37-26
WGK Germany 
3

MSDS

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Ethyl 2-oxo-4-phenylbutyrate Usage And Synthesis

synthesis

Potassium tert-butoxide (4.3 g, 38.34 mmol) was added in 1 portion to a solution of the diester (8 g, 25.56 mmol) in toluene (80 mL) at 0 °C. After being stirred at the same temperature for 30 min, the reaction mixture was kept at room temperature overnight. Water (100 mL) was added, the phases were separated, and the aqueous phase was extracted with EtOAc (3 × 100 mL). The combined organic extracts  were dried and evaporated. The residue was purifified by flflash chromatography  eluting with EtOAc:light petroleum (1:9) to give 5.6 g (78%) of the keto-ester as an orange oil.

Chemical Properties

light yellow oily liquid

Uses

Ethyl 2-oxo-4-phenylbutyrate may be used in the synthesis of ethyl (R)-2-hydroxy-4-phenylbutyrate, an important chiral precursor for angiotensin-converting enzyme (ACE) inhibitor.

General Description

Ethyl 2-oxo-4-phenylbutyrate is an aliphatic α-ketoester. Bioreduction of ethyl 2-oxo-4-phenylbutyrate is reported to yield ethyl (R)-2-hydroxy-4-phenylbutanoate. The effect of ionic liquid on the asymmetric reduction of ethyl 2-oxo-4-phenylbutyrate by Saccharomyces cerevisiae has been reported. Asymmetric reduction of ethyl 2-oxo-4-phenylbutyrate using a bacterial reductase is reported. Enantioselective hydrogenation of ethyl 2-oxo-4-phenylbutyrate using homogeneous Rh-diphosphine and heterogeneous Pt/Al2O3-cinchona catalysts has been reported.

Ethyl 2-oxo-4-phenylbutyrate Preparation Products And Raw materials

Preparation Products

Ethyl 2-oxo-4-phenylbutyrate Supplier

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