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[ CAS No. 175406-94-7 ] {[proInfo.proName]}

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Chemical Structure| 175406-94-7
Chemical Structure| 175406-94-7
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Product Details of [ 175406-94-7 ]

CAS No. :175406-94-7 MDL No. :MFCD20483492
Formula : C14H17NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :ZBQNYNWPYXTUTB-UHFFFAOYSA-N
M.W : 247.29 Pubchem ID :418617
Synonyms :

Safety of [ 175406-94-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 175406-94-7 ]

* 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.

  • Upstream synthesis route of [ 175406-94-7 ]
  • Downstream synthetic route of [ 175406-94-7 ]

[ 175406-94-7 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 175406-94-7 ]
  • [ 32018-96-5 ]
Reference: [1] Patent: CN103896826, 2016, B,
  • 2
  • [ 40114-49-6 ]
  • [ 616-38-6 ]
  • [ 175406-94-7 ]
YieldReaction ConditionsOperation in experiment
99% for 0.333333 h; Heating / reflux [0248] To a stirred mixture of l-benzylpiperidin-3-one (72 g) and dimethyl carbonate (500 mL) was added NaH (38 g, 60percent). After 20 minutes at reflux, water (800 mL) was added. The resulting solution was extracted with ethyl acetate (3 x 400 mL), dried over sodium sulfate and concentrated to give methyl l-benzyl-3- oxopiperidine-4-carboxylate as a brown oil (93 g, 99percent). LCMS: 248 (M+H) +.
Reference: [1] Patent: WO2009/26241, 2009, A1, . Location in patent: Page/Page column 77-78
  • 3
  • [ 67-56-1 ]
  • [ 39514-19-7 ]
  • [ 175406-94-7 ]
Reference: [1] Patent: WO2014/26330, 2014, A1, . Location in patent: Page/Page column 39-40
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