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Chemical Structure| 478841-09-7 Chemical Structure| 478841-09-7

Structure of 478841-09-7

Chemical Structure| 478841-09-7

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Product Details of [ 478841-09-7 ]

CAS No. :478841-09-7
Formula : C16H21NO3
M.W : 275.34
SMILES Code : O=C(C1C(CN(CC2=CC=CC=C2)CCC1)=O)OCC
MDL No. :MFCD28010090

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Application In Synthesis of [ 478841-09-7 ]

* 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 [ 478841-09-7 ]

[ 478841-09-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 478841-09-7 ]
  • [ 146407-32-1 ]
YieldReaction ConditionsOperation in experiment
89% With hydrogenchloride; for 12h;Reflux; Inert atmosphere; Compound 53-3 (18 g, 65.5 mmol) was added into HCl solution (6 mol/L, 180 mL) under nitrogen atmosphere, and the reaction solution was stirred at reflux for 12 h. After TLC indicated the reaction was complete, the reaction solution was cooled down to r.t. and adjusted to a pH greater than 9 with NaOH solution. The resulting solution was extracted with a mixture of DCM/MeOH (10/1) (200 mL×2). The organic phase was washed with saturated brine, dried over anhydrous Na2SO4, filtered and evaporated to give the title compound 53-4 (yellow oil, 11.9 g, Yield 89%). 1H NMR (400 MHz, d6-DMSO): delta ppm 7.38-7.27 (m, 5H), 3.72 (s, 2H), 3.27 (s, 2H), 2.76-2.71 (m, 4H), 1.75 (m, 4H)
With sulfuric acid; In ethanol; water; at 120℃; for 12h; Under a nitrogen atmosphere, a 75%-aqueous sulfuric acid solution (2 ml) was added to a solution of ethyl 1-benzyl-3-oxoazepane-4-carboxylate (150 mg, 0.545 mmol) in ethanol (1 ml) at room temperature, and the resulting mixture was heated to 120C. After 3 hours, completion of the reaction was confirmed and the resulting mixture was cooled. On the other hand, under a nitrogen atmosphere, a 75%-aqueous sulfuric acid solution (2 ml) was added to a solution of the mixture containing ethyl 1-benzyl-3-oxoazepane-2-carboxylate (200 mg, content = about 75%) in ethanol (1 ml) at room temperature, and the resulting mixture was heated to 120C. After 12 hours, completion of the reaction was confirmed and the temperature was lowered. The reaction solution was combined with that obtained above, and the combined reaction solution was poured onto ice and adjusted to pH 8 with a 2M-aqueous sodium hydroxide solution. The combined reaction solution thus treated was extracted with ethyl acetate (50 ml x 2) and the organic layer was dried over anhydrous magnesium sulfate. The organic layer dried was concentrated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate) to obtain 1-benzylazepan-3-one (118.1 mg, 53%).
 

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