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Chemical Structure| 116178-39-3 Chemical Structure| 116178-39-3

Structure of 116178-39-3

Chemical Structure| 116178-39-3

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Product Details of [ 116178-39-3 ]

CAS No. :116178-39-3
Formula : C7H9NO2
M.W : 139.15
SMILES Code : OC1=CC=C(OCC)N=C1
MDL No. :MFCD18819177

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Application In Synthesis of [ 116178-39-3 ]

* 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 [ 116178-39-3 ]

[ 116178-39-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34368-52-0 ]
  • [ 116178-39-3 ]
  • [ 1593701-18-8 ]
YieldReaction ConditionsOperation in experiment
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; for 2h;Inert atmosphere; (R)-3((6-Ethoxypyridin-3-yl)oxy)pyrrolidin-2-one A mixture of (S)-3-hydroxy-pyrrolidin-2-one (8.07 g), 6-ethoxypyridin-3-ol (11.0 g) and THF (100 mL) was purged with argon. Triphenylphosphine (20.7 g) was added followed by slow addition of DIAD (16.0 g). After 2 hours the mixture was concentrated and the residue purified by SGC (eluent: EA) to provide the subtitle compound. MS ESI+: m/z=223 [M+H]+.
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; for 2h;Inert atmosphere; A mixture of (S)-3-hydroxy-pyrrolidin-2-one (8.07 g), 6-ethoxypyridin-3-ol (1 1 .0 g) and THF (100 mL) was purged with argon. Triphenylphosphine (20.7 g) was added followed by slow addition of DIAD (16.0 g). After 2 hours the mixture was concentrated and the residue purified by SGC (eluent: EA) to provide the subtitle compound. MS EST: m/z = 223 [M+H]+.
 

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