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Chemical Structure| 53005-24-6 Chemical Structure| 53005-24-6

Structure of 53005-24-6

Chemical Structure| 53005-24-6

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Product Details of [ 53005-24-6 ]

CAS No. :53005-24-6
Formula : C13H27NO2
M.W : 229.36
SMILES Code : O=C(OC)CCCCCCCCCCCN

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Application In Synthesis of [ 53005-24-6 ]

* 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 [ 53005-24-6 ]

[ 53005-24-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 53005-24-6 ]
  • [ 67107-87-3 ]
YieldReaction ConditionsOperation in experiment
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0℃; for 48h;Reflux; Inert atmosphere; General procedure: Freshly distilled acetyl chloride (1.70 mL, 23.90 mmol) was added dropwise to a stirred suspension of 10-aminodecanoic acid 12 (1.80 g, 9.61 mmol) in anhydrous MeOH (20 mL) under N2 atmosphere at 0 C. Once the addition was complete, the mixture was heated under reflux for 3 h. After completion of the reaction, the solvent and excess acetyl chloride were distilled off under reduced pressure affording the corresponding methyl 10-aminodecanoate as a white solid (89%), which was used in the next reaction without further purification. Lithium aluminum hydride (1.65 g, 17.20 mmol) was added in small portions to a stirred suspension of the amino ester intermediate (1.73 g, 8.57 mmol) in anhydrous THF (100 mL) at 0 C. The reaction mixture was heated under reflux for 48 h, then cooled to room temperature and poured into crushed ice. The aqueous layer was vigorously extracted with CH2Cl2 (6 x 80 mL) and the combined organic phases were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure and the crude product was recrystallized to obtain pure 16 (0.92 g, 62%).
  • 2
  • [ 6404-26-8 ]
  • [ 53005-24-6 ]
  • C26H49N3O6 [ No CAS ]
 

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