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Chemical Structure| 119357-91-4 Chemical Structure| 119357-91-4

Structure of 119357-91-4

Chemical Structure| 119357-91-4

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Product Details of [ 119357-91-4 ]

CAS No. :119357-91-4
Formula : C14H15NO2
M.W : 229.27
SMILES Code : O=C(OC)[C@@H](N)CC1=C2C=CC=CC2=CC=C1
MDL No. :MFCD08058289

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Application In Synthesis of [ 119357-91-4 ]

* 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 [ 119357-91-4 ]

[ 119357-91-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 78306-92-0 ]
  • [ 119357-91-4 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In methanol; Example 85-1 Synthesis of methyl <strong>[78306-92-0]D-3-(1-naphthyl)alanine</strong> Methanol (1 ml) was cooled to -10C and thionyl chloride (0.091 g) was gradually added while stirring. After 10 minutes, commercially available <strong>[78306-92-0]D-3-(1-naphthyl)alanine</strong> (0.04569 g) was added. After stirring for 21 hours at room temperature, the reaction mixture was concentrated under reduced pressure. Methanol (12 ml) was added and the solvent was removed by distillation. The mixture obtained by repeating this procedure twice was fractioned into portions dissolvable into saturated sodium hydrogencarbonate aqueous solution and chloroform. The water layer was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed by distillation to obtain the title compound (40.3 mg) as a colorless liquid. MS(FAB,Pos.):m/z=230[M+1]+ 1H-NMR(500MHz,CDCl3):delta=3.14(1H,dd,J=13.9,8.8Hz),3.69(1H,dd, J=13.9,4.9Hz),3.91(1H,dd,J=8.8,4.9Hz),7.35(1H,d,6.1Hz),7.42 (1H,dd,7.1,1.0Hz),7.48-7.57(2H,m),7.78(1H,d,8.3Hz),7.87(1H,dd,J=8.1,1.2Hz),8.09(1H,d,J=8.5Hz).
 

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