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Chemical Structure| 887594-13-0 Chemical Structure| 887594-13-0

Structure of 887594-13-0

Chemical Structure| 887594-13-0

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Product Details of [ 887594-13-0 ]

CAS No. :887594-13-0
Formula : C11H16N2O3
M.W : 224.26
SMILES Code : O=C(N1CC(C(CC#N)=O)C1)OC(C)(C)C
MDL No. :MFCD06656778

Safety of [ 887594-13-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 887594-13-0 ]

* 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 [ 887594-13-0 ]

[ 887594-13-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 610791-05-4 ]
  • [ 75-05-8 ]
  • [ 887594-13-0 ]
YieldReaction ConditionsOperation in experiment
With potassium tert-butylate; In tetrahydrofuran; at 20℃; for 1h;Inert atmosphere; To an ice -cooled solution of 1-ieri-butyl 3-methyl azetidine-l,3-dicarboxylate (10.0 g, 46.5 mmol) and acetonitrile (2.9 g, 69.8 mmol) in tetrahydrofuran (250 mL) was added potassium ieri-butoxide (70 mL, 69.8 mmol) dropwise under the atmosphere of nitrogen. The resulting mixture was warmed to room temperature. After 1 h, the reaction mixture was poured into saturated aqueous ammonium chloride (500 mL), and the resulting solution was extracted with ethyl acetate (3 x 500 mL). The combined organic was washed with saturated aqueous sodium chloride solution (500 mL), dried over anhydrous sodium sulfate, and concentrated in vacuo (10 g, 96% crude yield). NMR (400 MHz, CDC13): delta 4.16 - 4.09 (m, 4 H), 3.72 - 3.64 (m, 1 H), 3.50 - 3.48 (m, 2 H), 1.43 (s, 9 H).
540 mg With potassium tert-butylate; In tetrahydrofuran; for 3.5h; (1) To a solution of <strong>[610791-05-4]1-tert-butyl 3-methyl azetidine-1,3-dicarboxylate</strong> (2.0 g) in THF (50 mL) were added acetonitrile (720 muL) and potassium tert-butoxide (1.6 g), and the mixture was stirred for 210 minutes. To the reaction solution was added an aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane) to obtain 540 mg of tert-butyl 3-(2-cyanoacetyl)azetidine-1-carboxylate. (2329) 1H-NMR (CDCl3): delta 1.44 (9H, s), 3.50 (2H, s), 3.66-3.72 (1H, m), 4.10-4.16 (4H, m)
  • 2
  • [ 610791-05-4 ]
  • [ 887594-13-0 ]
YieldReaction ConditionsOperation in experiment
1.2 g With sodium hydride; In tetrahydrofuran; acetonitrile; mineral oil; at 70℃;Inert atmosphere; To a solution of sodium hydride (60% in mineral oil, 2.8 g) in tetrahydrofuran (40 mL) was added dropwise a solution of <strong>[610791-05-4]1-tert-butyl 3-methyl azetidine-1,3-dicarboxylate</strong> (10 g) and acetonitrile (3.7 mL) in tetrahydrofuran (40 mL) at 70 C. under nitrogen atmosphere, and the mixture was stirred overnight at the same temperature. To the reaction mixture was added 1 M hydrochloric acid, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.2 g). (0990) MS (ESI-), found: 223.1
 

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