ChemicalBook > Product Catalog > Organic Chemistry > Carboxylic acids and derivatives > Ethyl 3-oxocyclohexane-1-carboxylate
Ethyl 3-oxocyclohexane-1-carboxylate
Ethyl 3-oxocyclohexane-1-carboxylate Basic information
- Product Name:
- Ethyl 3-oxocyclohexane-1-carboxylate
- Synonyms:
-
- ETHYL 3-OXOCYCLOHEXANE-1-CARBOXYLATE
- ETHYL 3-OXOCYCLOHEXANECARBOXYLATE
- 3-Cyclohexanonecarboxylic acid ethyl ester
- 3-Oxocyclohexane-1-carboxylic acid ethyl ester
- 3-Oxocyclohexanecarboxylic acid ethyl ester
- 1-(Ethoxycarbonyl)-3-oxocyclohexane, 3-(Ethoxycarbonyl)cyclohexan-1-one
- Ethyl 3-oxocyclohexane-1-carboxylate 97+%
- Ethyl 3-oxo-cyclohexane formate
- CAS:
- 33668-25-6
- MF:
- C9H14O3
- MW:
- 170.21
- EINECS:
- 251-626-8
- Product Categories:
-
- Esters
- Ring Systems
- Mol File:
- 33668-25-6.mol
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Ethyl 3-oxocyclohexane-1-carboxylate Chemical Properties
- Boiling point:
- 249℃
- Density
- 1.083
- Flash point:
- 104℃
- storage temp.
- 2-8°C
- InChI
- InChI=1S/C9H14O3/c1-2-12-9(11)7-4-3-5-8(10)6-7/h7H,2-6H2,1H3
- InChIKey
- YLRVJPQVDQQBOX-UHFFFAOYSA-N
- SMILES
- C1(C(OCC)=O)CCCC(=O)C1
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Ethyl 3-oxocyclohexane-1-carboxylate Usage And Synthesis
Uses
Ethyl Cyclohexanone-β-carboxylate is an intermediate used to prepare carbazole-carboxamides with selective JAK2 inhibitory activities.
Synthesis Reference(s)
Journal of the American Chemical Society, 110, p. 2565, 1988 DOI: 10.1021/ja00216a033
Synthesis
To a round bottom flask was added 3-oxo-1-cyclohexanecarboxylic acid (3.85 g, 27.1 mmol), ethanol (7.91 mL), p-toluenesulfonic acid (0.097 g, 0.56 mmol) and toluene (65.9 mL). The mixture was refluxed with a Dean-star trap overnight. The reaction mixture was cooled down and concentrated under reduced pressure to afford 4.61 g (100 %) of the title compound, 3-oxo-cyclohexanecarboxylic acid ethyl ester (Ethyl 3-oxocyclohexane-1-carboxylate), as a yellow oil.
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