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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  Ethyl 3-oxocyclohexane-1-carboxylate

Ethyl 3-oxocyclohexane-1-carboxylate

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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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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
Hazard Note 
Irritant
HS Code 
2918199890
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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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