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Chemical Structure| 211108-48-4 Chemical Structure| 211108-48-4

Structure of 211108-48-4

Chemical Structure| 211108-48-4

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Product Details of [ 211108-48-4 ]

CAS No. :211108-48-4
Formula : C13H25NO3Si
M.W : 271.43
SMILES Code : O=C(N1CCC(O[Si](C)(C)C)=CC1)OC(C)(C)C
MDL No. :MFCD09261243

Safety of [ 211108-48-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 211108-48-4 ]

* 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 [ 211108-48-4 ]

[ 211108-48-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 211108-48-4 ]
  • [ 188869-05-8 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; In tetrachloromethane; at 10 - 15℃; for 2h; To a stirred solution of tert-butyl-4-((trimethylsilyl)oxy)-3,6-dihydropyridine-1(2H)-carboxylate, obtained in step 1, (7.48 g, 27.60 mmol) in dry CCl4 (80 mL, 10 V), N-bromosuccinimide (5.42 g, 30.36 mmol) was added at 10 °C. The reaction mixture was stirred at 10-15 °C for 2 h. It was evaporated under reduced pressure. Water (30 mL) was added and the desired product was extracted with EtOAc (2x60 mL). Organic layer was dried over Na2SO4 and the solvents were evaporated. The resulting crude product was purified by flash chromatography affording the title product (white solid). 1H NMR (400 MHz, DMSO-d6): delta 4.74 (s, 1H), 4.02-4.00 (m, 2H), 3.60-3.58 (m, 2H), 2.69-2.68 (m, 2H), 1.39 (s, 9H).
With N-Bromosuccinimide; In tetrahydrofuran; at 0 - 20℃; Chlorotrimethylsilane (5.6 ml, 44 mmol) was added slowly to a solution of foert-butyl 4-oxopiperidine-l-carboxylate (8 g, 40 mmol), triethylamine (12.3 ml, 88 mmol) and DMF (40 ml) at room temperature. The resultant solution was heated to 75 °C and stirred overnight under nitrogen. The reaction mixture was cooled to room temperature and then in an ice bath. Cold hexane (250 ml) was added slowly to the reaction mixture followed by cold (saturated) aqueous sodium bicarbonate (50 ml). The organic phase was separated and washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude silyl enolether was dissolved in THF (15 ml) and cooled to 0 °C. JV-Bromosuccinimide (7.1 g, 40 mmol) was dissolved in THF (120 ml) and was added slowly (45 min.) to the reaction mixture. The resultant mixture was allowed to slowly warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure. The crude residue was purified by flash chromatography (hexanes/EtOAc, 5:1) to provide the title compound as a white solid (11 g). MS (ESP): 222.1 (M - t-Bu) for C10H16BrNO3; NMR: 1.25 (s, 9 H), 2.30 (m, 1 H), 2.55 (m, 1 H), 3.42-3.80 (m, 3 H), 3.93 (m, 1 H), 4.60 (m, 1 H).
 

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