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[ CAS No. 161157-50-2 ] {[proInfo.proName]}

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Chemical Structure| 161157-50-2
Chemical Structure| 161157-50-2
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Product Details of [ 161157-50-2 ]

CAS No. :161157-50-2 MDL No. :MFCD12407050
Formula : C10H17NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MMPWHAJQEZIIEH-UHFFFAOYSA-N
M.W : 199.25 Pubchem ID :21991116
Synonyms :

Safety of [ 161157-50-2 ]

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

Application In Synthesis of [ 161157-50-2 ]

* 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 [ 161157-50-2 ]

[ 161157-50-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 100-59-4 ]
  • [ 161157-50-2 ]
  • [ 1000931-04-3 ]
YieldReaction ConditionsOperation in experiment
94% According to Tetrahedron Lett., 1979, 17, 1503, to a stirred solution of phenylmagnesium chloride (0.753 mL, 1.51 mmol) and copper (I) iodide (0.0191 g, 0.100 mmol) in THF (3 mL) at -300C was added tert-butyl 7-oxa-3-aza- bicyclo[4.1.0]heptane-3-carboxylate (0.200 g, 1.00 mmol) in THF (1 mL) . The mixture was allowed to warm to room temperature and was stirred for 16 h. It was then quenched with saturated aqueous ammonium chloride and the mixture was extracted with AcOEt. The combined organic layers were dried (sodium sulfate) , filtered, and concentrated in vacuo to give tert-butyl 3-hydroxy-4-phenylpiperidine-l-carboxylate (0.261 g, 94%) as an oil: 1H NMR (400 MHz, DMSO-d6) delta 1-49 (s, 9H), 1.76 (m, 3H), 2.50-2.78 (m, 3H), 3.70 (m, IH), 4.30 (bd, IH), 7.30 (m, 5H).
  • 2
  • [ 161157-50-2 ]
  • [ 224779-27-5 ]
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