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Chemical Structure| 314732-37-1 Chemical Structure| 314732-37-1

Structure of 314732-37-1

Chemical Structure| 314732-37-1

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Product Details of [ 314732-37-1 ]

CAS No. :314732-37-1
Formula : C15H22N2O4
M.W : 294.35
SMILES Code : O=C(OC(C)(C)C)NCC1=CC=C(C(NCOC)=O)C=C1

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Application In Synthesis of [ 314732-37-1 ]

* 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 [ 314732-37-1 ]

[ 314732-37-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 314732-37-1 ]
  • [ 156866-52-3 ]
YieldReaction ConditionsOperation in experiment
85% With lithium aluminium tetrahydride; In tetrahydrofuran; at -78 - 4℃; for 4.41667h;Cooling with acetone-dry ice; tert- ut l 4-formylbenzyIcarbamate (Boc-Amb-H) Boc-Amb-N(OMe)Me (2.45 g, 8.33 mmol, 1 eq) was dissolved in THF (83 mL) and cooled to -78 °C in a dry ice/acetone bath. Lithium aluminum hydride (0.41 g, 10.83 mmol, 1.3 eq) was added in 2 portions over 5 minutes. After 50 minutes, the suspension was warmed to 4 °C in an ice bath. After 3.5 hours, the reaction was deemed complete by TLC (mini workup in 10percent potassium bisulfate and EtOAc, 50percent EtOAc hexanes) and the reaction was quenched by the slow addition of 10percent potassium bisulfate at 4 °C. The mixture was warmed to room temperature, and stirred for 30 minutes. Most of the THF was removed under reduced pressure and mixture was diluted with water and extracted thrice with EtOAc. The combined organic layer was washed once with brine, dried over sodium sulfate, filtered and condensed. Purification by column chromatography (40 to 50percent EtOAc/hexanes) gave Boc-Amb-H as a white solid (1.66 g, 7.1 mmol, 85percent). 1H NMR (500 MHz, CDC13) delta 9.96 (s, 1H), 7.81 (d, j = 8.2 Hz, 2H), 7.41 (d, J= 8.0 Hz, 2H), 5.12 (s, 1H), 4.37 (d, J= 5.6 Hz, 2H), 1.44 (s, 9H). 13C NMR (126 MHz, CDC13) 5 191.94, 156.03, 146.30, 135.62, 130.14, 127.78, 79.92, 44.44, 28.46. MS (ESI) 235.9 (M+H), 180.2 (M-tBu).
85% With lithium aluminium tetrahydride; In tetrahydrofuran; at -78 - 4℃; for 4.41h; Boc-Amb-N(OMe)Me (2.45 g, 8.33 mmol, 1 eq) was dissolved in THF (83 mL) and cooled to ?78° C. in a dry ice/acetone bath. Lithium aluminum hydride (0.41 g, 10.83 mmol, 1.3 eq) was added in 2 portions over 5 minutes. After 50 minutes, the suspension was warmed to 4° C. in an ice bath. After 3.5 hours, the reaction was deemed complete by TLC (mini workup in 10percent potassium bisulfate and EtOAc, 50percent EtOAc/hexanes) and the reaction was quenched by the slow addition of 10percent potassium bisulfate at 4° C. The mixture was warmed to room temperature, and stirred for 30 minutes. Most of the THF was removed under reduced pressure and mixture was diluted with water and extracted thrice with EtOAc. The combined organic layer was washed once with brine, dried over sodium sulfate, filtered and condensed. Purification by column chromatography (40 to 50percent EtOAc/hexanes) gave Boc-Amb-H as a white solid (1.66 g, 7.1 mmol, 85percent). 1H NMR (500 MHz, CDCl3) delta 9.96 (s, 1H), 7.81 (d, J=8.2 Hz, 2H), 7.41 (d, J=8.0 Hz, 2H), 5.12 (s, 1H), 4.37 (d, J=5.6 Hz, 2H), 1.44 (s, 9H). 13C NMR (126 MHz, CDCl3) delta 191.94, 156.03, 146.30, 135.62, 130.14, 127.78, 79.92, 44.44, 28.46. MS (ESI) 235.9 (M+H), 180.2 (M-tBu).
 

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