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Chemical Structure| 146059-76-9 Chemical Structure| 146059-76-9

Structure of 146059-76-9

Chemical Structure| 146059-76-9

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Product Details of [ 146059-76-9 ]

CAS No. :146059-76-9
Formula : C8H13NO3
M.W : 171.19
SMILES Code : CCOC(=O)C1CCC(=O)NC1
MDL No. :MFCD13179490

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Application In Synthesis of [ 146059-76-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 146059-76-9 ]

[ 146059-76-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22540-50-7 ]
  • [ 146059-76-9 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In ethanol; EXAMPLE 2 5-Ethoxycarbonyl-2-piperidone To a suspension of 250 g of <strong>[22540-50-7]5-carboxy-2-piperidone</strong> in 2.5 liters of punctilious ethanol were added 500 g of thionyl chloride at 22 C. Stir for 18 hours. The resulting solution was evaporated to dryness and the residue triturated with ether to give 233 g of the title compound: MS m/z 171 (M+), 142, 126, 115, 98; 300-MHz 1 H NMR (DMSO-d6) delta1.21 (t, J=7 Hz, 3 H), 1.78-1.92 (m, 1 H), 1.95-2.08 (m, 1 H), 2.15-2.31 (m, 2 H), 2.78-2.89 (m, 1 H), 3.25-3.40 (m, 2 H), 4.12 (t, J=7 Hz, 2 H), 7.95 (s, 1 H).
With thionyl chloride; In ethanol; at 0 - 20℃; for 24h; SOCl2 (2.93 g, 24.8 mmol) was dropped into a solution of <strong>[22540-50-7]6-oxopiperidine-3-carboxylic acid</strong> (1,72 g, 12.3 mmol) in (50 mL) at 0 C. Then the reaction was stirred at room temperature for 24 hours.The reaction mixtures was concentratedand the residue was triturated with ether to give white solid. MS (m/z): 172 (M+H)+
 

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