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Chemical Structure| 56880-02-5 Chemical Structure| 56880-02-5

Structure of 56880-02-5

Chemical Structure| 56880-02-5

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Product Details of [ 56880-02-5 ]

CAS No. :56880-02-5
Formula : C9H13NO2
M.W : 167.21
SMILES Code : O=C1CC(N2C(C)=O)CCC2C1

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Application In Synthesis of [ 56880-02-5 ]

* 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 [ 56880-02-5 ]

[ 56880-02-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25602-68-0 ]
  • [ 108-24-7 ]
  • [ 56880-02-5 ]
YieldReaction ConditionsOperation in experiment
0.7 g at 70℃; for 3h; Acetyl-8-aza-bicyclo[3.2.1 ]octan-3-one (4a)According to Scheme 2, Step 1 :A suspension of <strong>[25602-68-0]nortropinone hydrochloride</strong> (1 g, 6.187 mmol) in acetic anhydride was stirred at 70°C for 3h. Water was added, the mixture was boiled for 30 min and cooled down to room temperature. CH2CI2 and 1 N aqueous NaOH was added until pH 9 was reached. The mixture was extracted 2 times with CH2CI2, the combined organic layers were dried over Na2S04, filtrated and the solution was evaporated to dryness to give 0.7 g of 8-Acetyl-8-aza-bicyclo[3.2.1 ]octan-3-one (4a).Rt = 1 .76 min (LC-method 2). Detected mass: 168.24 [M+H+]
0.7 g at 70℃; for 3h; According to Scheme 2, Step 1 :A suspension of <strong>[25602-68-0]nortropinone hydrochloride</strong> (1 g, 6.187 mmol) in acetic anhydride was stirred at 70°C for 3h. Water was added, the mixture was boiled for 30 min and cooled down to room temperature. CH2CI2 and 1 N aqueous NaOH was added until pH 9 was reached. The mixture was extracted 2 times with CH2CI2, the combined organic layers were dried over Na2SO4, filtrated and the solution was evaporated to dryness to give 0.7 g of 8-Acetyl-8-aza-bicyclo[3.2.1 ]octan-3-one (4a).Rt = 1 .76 min (LC-method 2). Detected mass: 168.24 [M+H+]
0.7 g at 70℃; for 3h; According to Scheme 2, Step 1: A suspension of <strong>[25602-68-0]nortropinone hydrochloride</strong> (1 g, 6.187 mmol) in acetic anhydride was stirred at 70° C. for 3 h. Water was added, the mixture was boiled for 30 min and cooled down to room temperature. CH2Cl2 and 1N aqueous NaOH was added until pH 9 was reached. The mixture was extracted 2 times with CH2Cl2, the combined organic layers were dried over Na2SO4, filtrated and the solution was evaporated to dryness to give 0.7 g of 8-Acetyl-8-aza-bicyclo[3.2.1]octan-3-one (4a). Rt=1.76 min (LC-method 2). Detected mass: 168.24 [M+H+]
 

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