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Chemical Structure| 467454-33-7 Chemical Structure| 467454-33-7

Structure of 467454-33-7

Chemical Structure| 467454-33-7

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Product Details of [ 467454-33-7 ]

CAS No. :467454-33-7
Formula : C10H17NO2
M.W : 183.25
SMILES Code : O=C(N1C(C2)CC2C1)OC(C)(C)C
MDL No. :MFCD23131242

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Application In Synthesis of [ 467454-33-7 ]

* 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 [ 467454-33-7 ]

[ 467454-33-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 871658-02-5 ]
  • [ 24424-99-5 ]
  • [ 467454-33-7 ]
YieldReaction ConditionsOperation in experiment
88% With sodium hydroxide; In 1,4-dioxane; water; at 0 - 20℃; for 19.0h; To a solution of <strong>[871658-02-5]2-azabicyclo[2.1.1]hexane hydrochloride</strong> (20.0 g, 159 mmol) in 1,4-dioxane (300 mL) and water (300 mL) cooled to 0 C was added sodium hydroxide (1 mol/L) in water (318 mL, 318 mmol). Di -tert-butyl di carbonate (75 mL, 318 mmol) was then added by addition funnel over 30 min. The reaction was stirred at 0C for 30 min then warmed to room temperature and stirred for 18 h. The reaction mixture was concentrated in vacuo to remove dioxane and the aqueous residue was extracted with petroleum ether (3x). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was adsorbed onto silica and purified by flash column chromatography with 0-50% EtOAc in heptane to yield the title compound as a pale yellow solid (25.7 g, 88%). NMR (400 MHz, CDC13) delta 4.34 (s, 1H), 3.29 (s, 2H), 2.86 - 2.77 (m, 1H), 1.92 - 1.83 (m, 2H), 1.47 (s, 9H), 1.42 - 1.31 (m, 2H).
76% With sodium hydroxide; In 1,4-dioxane; water; at 20℃;Inert atmosphere; To a 2 L round-bottomed flask purged and maintained with an atmosphere of nitrogen was added <strong>[871658-02-5]2-azabicyclo[2.1.1]hexane hydrochloride</strong> (50.0 g, 418 mmol), 1,4-dioxane (420 mL), 1M aqueous sodiumhydroxide (840 mL) and di-tert-butyl dicarbonate (183 g). The resulting solution was stirred at roomtemperature overnight and then concentrated to remove organic solvent. The remaining slurry was extractedwith petroleum ether (3×500 mL). The combined organic layers were dried over anhydrous sodium sulfate andconcentrated. The residue was purified via flash column chromatography on silica gel (10:1 - 1:0 petroleumether/ethyl acetate) to afford tert-butyl 2-azabicyclo[2.1.1]hexane-2-carboxylate as an orange solid (58 g, 76%);
 

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