Basic information Safety Supplier Related

3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER

Basic information Safety Supplier Related

3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Basic information

Product Name:
3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
Synonyms:
  • 3-(3-bromophenyl)-3-keto-propionic acid ethyl ester
  • ETHYL 3-(3-BROMOPHENYL)-3-OXOPROPANOATE
  • ETHYL (3-BROMOBENZOYL)ACETATE
  • 3-Bromo--oxo-benzenepropanoic acid ethyl ester
  • 2-[(3-bromophenyl)-oxomethyl]butanoate
  • Ethyl (3-bromobenzoyl)acetate 95%
  • 3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
  • Benzenepropanoic acid,3-bromo-b-oxo-, ethyl ester
CAS:
21575-91-7
MF:
C11H11BrO3
MW:
271.11
Product Categories:
  • C10 to C11
  • Carbonyl Compounds
  • Esters
Mol File:
21575-91-7.mol
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3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Chemical Properties

Boiling point:
255-256 °C(lit.)
Density 
1.416 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.565(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
pka
9.91±0.46(Predicted)
Appearance
Light brown to reddish brown Liquid
CAS DataBase Reference
21575-91-7(CAS DataBase Reference)
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Safety Information

WGK Germany 
3

MSDS

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3-(3-BROMO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Usage And Synthesis

Uses

Reactant involved in synthesis of:

  • Aroylbenzoxepinones for analgesic activity
  • (Heteroaryl)(carboxamido)arylpyrrole derivatives with Cdc7 kinase inhibitory activity
  • Cambinol analogs for sirtuin inhibition and antitumor activity
  • TunePhos-type diphosphine ligands via asymmetric hydrogenation

Synthesis

24398-88-7

141-78-6

21575-91-7

A solution of 1.3 M LHMDS (25 mL, 32.7 mmol) in THF (10 mL) was stirred at -78 °C and under an inert atmosphere, and ethyl acetate (1.9 g, 21.8 mmol) was added slowly. After stirring for 15 min, ethyl 3-bromobenzoate (5 g, 21.8 mmol) was added and stirring was continued for 2 hours. The reaction progress was monitored by TLC. Upon completion of the reaction, the reaction was quenched with 10 mL of saturated aqueous NH4Cl and extracted with ethyl acetate (3 x 20 mL). The organic phases were combined, dried with anhydrous Na2SO4 and concentrated under reduced pressure to obtain the crude product. The crude product was purified by silica gel column chromatography with 4% ethyl acetate/hexane as eluent to afford the target compound, ethyl 3-bromobenzoylacetate (4.5 g, 76.9%) as a mixture of enol forms in the form of a brown oil.1H NMR (500 MHz, CDCl3): δ 8.07 (s, 1H), 7.86 (d, J=7.5 Hz, 1H), 7.73 -7.69 (m, 1H), 7.37 (t, J=7.0Hz, 1H), 4.28-4.26 (m, 2H), 3.92 (s, 2H), 1.24 (t, J=6.2Hz, 3H).MS (ESI): m/z 298.8 [M-1].

References

[1] Patent: WO2015/191630, 2015, A1. Location in patent: Paragraph 00457
[2] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2991 - 3013

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