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Chemical Structure| 5410-10-6 Chemical Structure| 5410-10-6

Structure of 5410-10-6

Chemical Structure| 5410-10-6

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Product Details of [ 5410-10-6 ]

CAS No. :5410-10-6
Formula : C8H13NO5
M.W : 203.19
SMILES Code : O=C(OC)CN(C(C)=O)CC(OC)=O
MDL No. :MFCD11501644

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Application In Synthesis of [ 5410-10-6 ]

* 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 [ 5410-10-6 ]

[ 5410-10-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 39987-25-2 ]
  • [ 108-24-7 ]
  • [ 5410-10-6 ]
YieldReaction ConditionsOperation in experiment
82% With triethylamine; at 0 - 20℃; for 4.5h; Acetic anhydride (9.1 ml, 96.7 mmol) was added dropwise at 0Cinto a solution <strong>[39987-25-2]dimethyl 2,2'-azanediyldiacetate hydrochloride</strong>4(14.70 g, 74.39 mmol) in triethylamine (50 ml). The reaction mixture was stirred for 0.5 h and then transferred to room temperature and stirred for 4 h. Triethylamine was removed under vacuum. The residue was extracted with dichloromethane and the organic phase was washed with saturated sodium chloride, dried over anhydrous sodium sulfate and concentrated. The crude product was purified by recrystallization from dichloromethane / n-hexane to give the compound5(12.39 g, 82%yield) as a white solid.1H NMR (500 MHz, CDCl3) delta 4.20 (s, 2H), 4.15 (s, 2H), 3.78 (s, 3H), 3.72 (s,3H), 2.12 (s, 3H). HRMS (ESI) (m/z):calcdfor C8H13NO5[M+H]+ 204.0872, found. 204.0864. [M+Na]+ 226.0691, found.226.0681.
82% With triethylamine; at 0 - 20℃; for 4.5h; Compound 2 (14.70 g, 74.39 mmol) was dissolved in 50 ml of triethylamine. The reaction solution was placed in an ice bath at 0 C, and acetic anhydride (9.1 ml, 96.7 mmol) was added. After 0.5 h of reaction, it was transferred to room temperature and stirred at room temperature for 4 h. Remove the solvent by spin. The reaction solution was extracted with dichloromethane / water. The dichloromethane phase was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated by rotary evaporation. The crude product was recrystallized from dichloromethane / n-hexane to give Compound 3 (12.39 g, 82%) as a white solid.
 

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