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Chemical Structure| 911102-04-0 Chemical Structure| 911102-04-0

Structure of 911102-04-0

Chemical Structure| 911102-04-0

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Product Details of [ 911102-04-0 ]

CAS No. :911102-04-0
Formula : C15H24N2O8
M.W : 360.36
SMILES Code : CC(C)(OC(NCCOCCOCC(ON1C(CCC1=O)=O)=O)=O)C
MDL No. :MFCD31381636

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Application In Synthesis of [ 911102-04-0 ]

* 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 [ 911102-04-0 ]

[ 911102-04-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6066-82-6 ]
  • [ 108466-89-3 ]
  • [ 911102-04-0 ]
YieldReaction ConditionsOperation in experiment
96% With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20℃; for 16h;Inert atmosphere; To a round bottom flask were added acid 33 (640 mg, 2.43 mmol), N- hydroxysuccinimide (419 mg, 3.64 mmol), DMAP (30 mg, 0.25 mmol), and 10 mL CH2CI2 under N2. The mixture was cooled down to 0 C and then a solution of DCC (752 mg, 3.64 mmol) in 10 mL CH2CI2 was added dropwise. The mixture was allowed to warm up to room temperature slowly overnight (16 h). Lots of white precipitates formed during the reaction. The precipitates were filtered off and the filtrate was washed with 20 mL 0.05 N HCl(aq) twice. The organic layer was dried with Na2S04 and concentrated under vacuum. The residue was dispersed in 20 mL EtOAc, and the insoluble precipitates were filtered off. The filtrate was concentrated to give T2 as a colorless oil (840 mg, 96%). NMR (400 MHz, CDCL): d 4.99 (s, 1H), 4.51 (s, 2H), 3.81-3.64 (m, 4H), 3.54 (t, J= 5.2 Hz, 2H), 3.32 (br q, J= 5.2 Hz, 2H), 2.86 (s, 4H), 1.44 (m, 9H).
91% With diisopropyl-carbodiimide; In tetrahydrofuran; at 20℃; for 2h; Boc-AEEA-OH (26.4 g, 100 mmol) and HOSu (12.6 g, 110 mmol) were dissolved in 200 ml tetrahydrofuran. DIC (13.9 g, 110 mmol) was added dropwise under a condition of ice bath, and the reaction was continued at room temperature for 2 h after the dropwise addition. TLC showed that the reaction of the raw materials was completed. A vacuum concentration was performed, and the residue was recrystallized with EA to obtain 33.0 g of Boc-AEEA-OSu with yield: 91%, purity: 96.7%, MS: 361.4 (M+1).
 

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