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Structure of 219617-08-0

Chemical Structure| 219617-08-0

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Product Details of [ 219617-08-0 ]

CAS No. :219617-08-0
Formula : C16H27NO8
M.W : 361.39
SMILES Code : O=C(OC)[C@@H](N(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O)CC(OC)=O

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Application In Synthesis of [ 219617-08-0 ]

* 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 [ 219617-08-0 ]

[ 219617-08-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 24424-99-5 ]
  • [ 130622-08-1 ]
  • [ 219617-08-0 ]
YieldReaction ConditionsOperation in experiment
100% With dmap; In acetonitrile; at 20℃; for 27h;Inert atmosphere; Dimethyl (2S)-2-(tert-butoxycarbonylamino)butane-1,4-dioate (0.90 g, 3.50 mmol) (6) was dissolved in acetonitrile (50 mL). 4-Dimethylaminopyridine (0.08 g, 0.70 mmol) and di-tert-butyl dicarbonate (0.80 g, 3.80 mmol) were added and the reaction mixture was allowed to stir at room temperature for 3 h. A further quantity of di-tert-butyl dicarbonate (0.40 g, 1.90 mmol) was added and the mixture was allowed to stir at room temperature for 24 h. The solvent was removed in vacuo and the crude product was purified using flash column chromatography (20% ethyl acetate in petroleum ether) to yield dimethyl (2S)-2-(di-tert-butoxycarbonylamino)butane-1,4-dioate (7) as a white solid (1.25 g, 100%). Mp 55-57 C; numax (NaCl) 2857 (CH), 1747 (C=O), 1458, 1375, 1145 cm-1; [alpha]D25 -61.5 (c 2.0, CHCl3), lit. 9a [alpha]D25 -61.0 (c 2.0, CHCl3); deltaH (400 MHz, CDCl3) 1.53 (18H, s, 2*tBu), 2.77 (1H, dd, J 16.4, 6.4 Hz, 3-HH), 3.29 (1H, dd, J 16.4, 7.2 Hz, 3-HH), 3.73 (3H, s, OMe), 3.76 (3H, s, OMe), 5.48 (1H, dd, J 7.2, 6.4 Hz, 2-H); deltaC (101 MHz, CDCl3) 28.0 (6*CH3), 35.7 (CH2), 52.0 (CH3), 52.6 (CH3), 54.9 (CH), 83.6 (2*C), 151.6 (2*C), 170.3 (C), 171.1 (C); m/z (CI) 362 (MH+, 6%), 306 (38), 250 (33), 206 (100), 162 (50); HRMS (CI): MH+, found 362.1819. C16H28NO8 requires 362.1815.
With dmap; In acetonitrile; at 0 - 20℃; for 18h; A 0 C solution of ()-dimethyl 2-((tert-butoxycarbonyl)amino)succinate (15.8 g, 60.5 mmol) in acetonitrile (200 mL) was treated with di-t-butyl dicarbonate (13.9 g, 63.5 mmol) and 4-dimethylaminopyridine (1.48 g, 12.1 mmol). The cooling bath was removed and the reaction solution stirred at ambient temperature overnight (18 h). The resulting solution was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL), washed with 0.25 N aqueous hydrochloric acid (2x50 mL), 0.25N aqueous sodium hydroxide (2x50 mL), and brine (1x50 mL); dried over magnesium sulfate and concentrated under reduced pressure to afford (S)- dimethyl 2-[bis(tert-butoxycarbonyl)amino]butane-l ,4-dioate (18.8 g, 52.0 mmol, 86% crude yield) as a pale yellow oil. The crude product was used without further purification. 1H NMR (400MHz, CDCh) delta ppm 5.46 (t, J=6.8 Hz, 1H), 3.72 (s, 3H), 3.74 (s, 3H), 3.26 (dd, J=16.4, 7.2 Hz, IH), 2.75 (dd, J=16.3, 6.5 Hz, IH), 1.52 (s, 18H).
With dmap; In acetonitrile; at 0 - 20℃; A 0 C solution of (S)-dimethyl 2-((tert-butoxycarbonyl)amino)succinate (15.8 g, 60.5 mmol) in acetonitrile (200 mL) was treated with di-t-butyl dicarbonate (13.9 g, 63.5 mmol) and 4-dimethylaminopyridine (1.48 g, 12.1 mmol). The cooling bath was removed and the reaction solution stirred at ambient temperature overnight (18 h). The resulting solution was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL), washed with 0.25 N aqueous hydrochloric acid (2x50 mL), 0.25N aqueous sodium hydroxide (2x50 mL), and brine (1x50 mL); dried over magnesium sulfate and concentrated under reduced pressure to afford (S)-dimethyl 2-[bis(tert-butoxycarbonyl)amino]butane-l,4-dioate (18.8 g, 52.0 mmol, 86% crude yield) as a pale yellow oil. The crude product was used without further purification.
  • 3
  • [ 130622-08-1 ]
  • [ 219617-08-0 ]
 

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