| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
sales8178@energy-chemical.com |
| Company Name: |
BePharm Ltd |
| Tel: |
400-685-9117 |
| Email: |
market@bepharm.com |
|
| | methyl 2-cyclohexyl-2-oxoacetate Basic information |
| | methyl 2-cyclohexyl-2-oxoacetate Chemical Properties |
| Boiling point | 50-52 °C(Press: 0.3 Torr) | | density | 1.079±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | Appearance | Colorless to light yellow Liquid |
| | methyl 2-cyclohexyl-2-oxoacetate Usage And Synthesis |
| Synthesis Reference(s) | Tetrahedron Letters, 18, p. 2825, 1977 DOI: 10.1016/S0040-4039(01)83085-9 | | Synthesis | To a methanol (5 mL) solution of 1-chloro-2-cyclohexylethane (0.50 mmol, purchased from ChemSampCo, Inc.) was added a water (5 mL) solution of sodium bicarbonate (23 mg, 0.28 mmol) and magnesium sulfate (135 mg, 1.10 mmol). The reaction mixture was stirred vigorously at 0°C for 10 min, followed by the addition of potassium permanganate (260 mg, 1.70 mmol). The mixture was warmed to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the solid residue was removed by filtration through a diatomaceous earth pad and the filter cake was washed with ethyl acetate. The organic phase was separated and the aqueous phase was extracted with ethyl acetate (3 x 100 mL). The organic phases were combined, washed with brine (30 mL) and dried with magnesium sulfate. The organic phases were concentrated and purified by fast column chromatography (eluent: hexane/ethyl acetate, 5:1) to afford the target product methyl 2-cyclohexyl-2-oxoacetate (78 mg, 90% yield). Thin Layer Chromatography (TLC, Expanding Agent: Hexane/Ethyl Acetate, 5:1): Rf = 0.40. Mass Spectrometry (ESI) m/z: 171.49 [M + H]+ (Calculated value: 171.16 [M + H]+). | | References | [1] Patent: WO2013/91900, 2013, A1. Location in patent: Page/Page column 36 |
| | methyl 2-cyclohexyl-2-oxoacetate Preparation Products And Raw materials |
|