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Chemical Structure| 285984-22-7 Chemical Structure| 285984-22-7

Structure of 285984-22-7

Chemical Structure| 285984-22-7

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Product Details of [ 285984-22-7 ]

CAS No. :285984-22-7
Formula : C15H17NO3
M.W : 259.30
SMILES Code : O=C(OC(C)(C)C)NC1=C2C=CC=CC2=C(O)C=C1
MDL No. :MFCD04114912

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Application In Synthesis of [ 285984-22-7 ]

* 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.

  • Downstream synthetic route of [ 285984-22-7 ]

[ 285984-22-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5344-27-4 ]
  • [ 285984-22-7 ]
  • [ 285984-36-3 ]
  • 2
  • [ 5344-27-4 ]
  • [ 285984-22-7 ]
  • [ 1972-28-7 ]
  • [ 607-52-3 ]
YieldReaction ConditionsOperation in experiment
With triphenylphosphine;N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; The product is then purified by column chromatography on silica gel, and reacted with a slight excess of phenyl chloroformate in the presence of N,N-diisopropyl-ethyl amine to afford the desired carbamate. To a solution of N-Boc-4-amino-naphthalene-1-ol (0.962 g), 2-(pyridin-4-yl)ethanol (1.4 g) and triphenylphosphine (2.90 g) in THF (25 mL) was added dropwise diethyl azodicarboxylate (1.8 mL). The mixture was stirred overnight and the volatiles removed in vacuo. Purification of the residue with flash chromatography using EtOAc as the eluent and concentration in vacuo of the product-rich fractions provided the desired naphthyl ether.
With triphenylphosphine;N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; The product is then purified by column chromatography on silica gel, and reacted with a slight excess of phenyl chloroformate in the presence of N,N-diisopropyl-ethyl amine to afford the desired carbamate. To a solution of N-Boc-4-amino-naphthalene-1-ol (0.962 g), 2-(pyridin-4-yl)ethanol (1.4 g) and triphenylphosphine (2.90 g) in THF (25 mL) was added dropwise diethyl azodicarboxylate (1.8 mL). The mixture was stirred overnight and the volatiles removed in vacuo. Purification of the residue with flash chromatography using EtOAc as the eluent and concentration in vacuo of the product-rich fractions provided the desired naphthyl ether.
 

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