ChemicalBook--->CAS DataBase List--->26510-52-1

26510-52-1

26510-52-1 Structure

26510-52-1 Structure
IdentificationBack Directory
[Name]

ETHYL PICOLINOYLACETATE
[CAS]

26510-52-1
[Synonyms]

BUTTPARK 18\10-45
ETHYL PICOLINOYLACETATE
ETHYL-2-PYRIDOYL ACETATE
Ethyl picolinoylacetate,95%
Ethyl 3-oxo-3-(pyridin-2-yl)
Ethyl picolinoylacetate, 95% 2.5GR
ETHYL 3-OXO-3-(2-PYRIDYL)PROPIONATE
Ethyl 3-(2-pyridyl)-3-oxopropionate
Ethyl 3-oxo-3-(2-pyridyl)propionate, 95+%
2-Pyridinepropanoic acid, β-oxo-, ethyl ester
ethyl 3-oxo-3-(2-pyridinyl)propanoate(SALTDATA: FREE)
Ethyl picolinoylacetate, Ethyl 3-oxo-3-(pyridin-2-yl)propionate, 2-(3-Ethoxy-3-oxopropanoyl)pyridine
[Molecular Formula]

C10H11NO3
[MDL Number]

MFCD00094022
[MOL File]

26510-52-1.mol
[Molecular Weight]

193.2
Chemical PropertiesBack Directory
[Appearance]

Clear straw-yellow to brown liquid
[Boiling point ]

100-104 °C (0.3 mmHg)
[density ]

1.164
[refractive index ]

1.516-1.519
[Fp ]

121℃
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Liquid
[pka]

9.37±0.46(Predicted)
[color ]

Clear straw-yellow to brown
[Sensitive ]

Light Sensitive
[CAS DataBase Reference]

26510-52-1
Hazard InformationBack Directory
[Chemical Properties]

Clear straw-yellow to brown liquid
[Synthesis]

Ethyl picolinate

2524-52-9

Ethyl acetate

141-78-6

ETHYL PICOLINOYLACETATE

26510-52-1

In a 22 L three-necked flask equipped with a reflux condenser tube, a nitrogen introduction tube and a mechanical stirrer, sodium ethoxide (360 g, 5.29 mol), toluene (4 L), ethanol (18 mL, 0.265 mol) and ethyl acetate (1.04 L, 10.6 mol) were added sequentially and stirring was initiated. After stirring for 1 h, the reaction mixture was warmed up to 26 °C. Subsequently, ethyl 2-pyridinecarboxylate (Fluka; 400 g, 2.65 mol) was added to the reaction system and the mixture was heated to reflux (90 °C) and maintained for 18 hours. After completion of the reaction, the mixture was cooled to room temperature, diluted with toluene (8 L) and subsequently washed with deionized water (6 L) and partitioned. The aqueous layer was adjusted to pH 5 with glacial acetic acid and extracted with ethyl acetate (2 x 4 L). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 466 g (91% yield) of the target product ethyl 3-oxo-3-(2-pyridinyl)propionate as a dark-colored oil, with a purity of 93% by HPLC analysis. Mass spectrum (ES+) m/e: 194 ([M+H]+).

[References]

[1] Patent: WO2005/92894, 2005, A1. Location in patent: Page/Page column 22
[2] Asian Journal of Chemistry, 2015, vol. 27, # 5, p. 1667 - 1670
[3] Patent: US2007/203154, 2007, A1. Location in patent: Page/Page column 54-55
[4] Helvetica Chimica Acta, 1955, vol. 38, p. 1289
[5] Journal of the American Chemical Society, 1948, vol. 70, p. 2755,2757
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

24/25-22-26
[Hazard Note ]

Irritant
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl acetate-->Sodium-->Ethyl picolinate-->Methyl picolinate-->Toluene-->Ethanol-->Sodium ethoxide
[Preparation Products]

2-Pyridylethylamine-->2-methyl-6-(pyridin-2-yl)pyrimidin-4-ol-->1H-Pyrazol-5-ol, 1-ethyl-3-(2-pyridinyl)-
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL PICOLINOYLACETATE(26510-52-1)1HNMR
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