Ethyl 2-oxohexanoate
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
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
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
Ethyl 2-oxohexanoateSupplier
- Tel
- 13913622609
- 974295387@qq.com
- Tel
- 0311-89250318 031166536426
- master@sjzsdyn.com
- Tel
- +86 (0) 571 85 58 67 18
- Tel
- 13817811078
- sales@jingyan-chemical.com
- Tel
- 021-54306202 13764082696
- info@hanhongsci.com
Ethyl 2-oxohexanoate(5753-96-8)Related Product Information
- Nalidixic acid
- Trinexapac-ethyl
- Tris(trimethylsilyl)phosphate
- Ethanol
- Ethyl formate
- Ethylparaben
- ISOXADIFEN-ETHYL
- Ethyl 6-bromohexanoate
- PICROLONIC ACID
- Ethyl propiolate
- Ethyl Hexanoate
- Diethylstilbestrol
- Methyl dihydrojasmonate
- 2-Hexanone
- Methyl acrylate
- Ethyl acrylate
- Ethyl cyanoacetate
- Ethyl acetate