Basic information Safety Supplier Related

Ethyl 2-oxohexanoate

Basic information Safety Supplier Related

Ethyl 2-oxohexanoate Basic information

Product Name:
Ethyl 2-oxohexanoate
Synonyms:
  • 2-oxohexanoic acid ethyl ester
  • ethyl alpha-ketocaproate
  • Ethyl 2-oxohexanoate
  • 2-Ketocaproic acid ethyl ester
  • 2-Oxyhexanoic acid ethyl ester
  • 2-ketoHexanoicacidethylester
  • Hexanoic acid, 2-oxo-, ethyl ester
  • Ethyl 2-oxohexanoate - [E12153]
CAS:
5753-96-8
MF:
C8H14O3
MW:
158.2
EINECS:
1308068-626-2
Product Categories:
  • API
Mol File:
5753-96-8.mol
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Ethyl 2-oxohexanoate Chemical Properties

Boiling point:
96°C
Density 
0.981
Flash point:
81°C
storage temp. 
Sealed in dry,Room Temperature
Appearance
Light yellow to green yellowLiquid
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Safety Information

HS Code 
2918300090
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Ethyl 2-oxohexanoate Usage And Synthesis

Chemical Properties

Pale yellow liquid

Synthesis Reference(s)

The Journal of Organic Chemistry, 29, p. 2080, 1964 DOI: 10.1021/jo01030a549

Synthesis

92273-73-9

4755-77-5

5753-96-8

General procedure for the synthesis of ethyl 2-oxohexanoate from n-butylzinc bromide and monoethyl oxalyl chloride: a stirred solution of copper iodide (2.29 g, 12 mmol) in anhydrous tetrahydrofuran was cooled to -25 °C and a tetrahydrofuran solution of 0.5 M n-butylzinc bromide (24 mL, 12 mmol) was added slowly dropwise. After addition, the reaction mixture was warmed to 0 °C and stirred at that temperature for 20 min, then cooled to -25 °C again. The reaction mixture was treated dropwise with monoethyl oxalyl chloride (1.37 g, 10 mmol). After stirring at -25 °C for 3 h, the reaction mixture was warmed to room temperature, the reaction was quenched with saturated aqueous ammonium chloride solution and the aqueous layer was extracted with ether. The combined organic phases were washed with brine, filtered, dried over anhydrous sodium sulfate and concentrated in vacuum. The crude product was purified by ISCO fast column chromatography using a pre-populated RediSep silica gel column (gradient elution, 0→20% ethyl acetate in hexane solution) to afford ethyl 2-oxohexanoate (0.60 g, 37%) as a colorless oil.1H NMR (400 MHz, CDCl3) δ 0.91-0.98 (3H, m), 1.34- 1.47 (5H, m), 1.58-1.76 (2H, m), 2.83 (1H, t, J = 7.3 Hz), 4.27-4.37 (2H, m).

References

[1] Patent: US2008/90814, 2008, A1. Location in patent: Page/Page column 23-24

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