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Chemical Structure| 848440-23-3 Chemical Structure| 848440-23-3

Structure of 848440-23-3

Chemical Structure| 848440-23-3

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Product Details of [ 848440-23-3 ]

CAS No. :848440-23-3
Formula : C11H13BrFNO2
M.W : 290.13
SMILES Code : O=C(OC(C)(C)C)NC1=CC=CC(Br)=C1F

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Application In Synthesis of [ 848440-23-3 ]

* 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 [ 848440-23-3 ]

[ 848440-23-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 161957-56-8 ]
  • [ 75-65-0 ]
  • [ 848440-23-3 ]
YieldReaction ConditionsOperation in experiment
61% A suspension of <strong>[161957-56-8]3-bromo-2-fluorobenzoic acid</strong> (21.9 g, 100 mmol), DPPA (33.0 g, 120 mmol), and triethylamine (17 mL, 120 mmol) in toluene (1,000 mL) was stirred at 120C. After the mixture was heated to reflux for 2 hours, t-BuOH was added to the mixture, and the mixture was heated to reflux for further 2 hours. The solvent was removed from the mixture, the residue was purified by silica gel column chromatography using petroleum ether to give tert-butoxy-N-(3-bromo-2-fluorophenyl)carboxamide as colorless oil (17.7 g, yield 61%). 1H-NMR Spectrum (300MHz, CDCl3):δ (ppm): 1.52 (s, 3H), 6.72 (brs, 1H), 6.93-6.99 (m, 1H), 7.12-7.18 (m, 1H), 8.04 (t, J=7.5Hz, 1H)
Triethylamine (0.6 ml) was added to a stirred solution of <strong>[161957-56-8]3-bromo-2-fluorobenzoic acid</strong> (438 mg, 2MMOL) in tert-butanol (10 ml). Diphenyl phosphoryl azide (1 ml, 4. 6MMOL) was then added and the reaction mixture was heated under reflux overnight. The solution was evaporated to dryness and azeotroped with toluene. The residues were then purified by flash chromatography on silica eluting with ethyl acetate/i-hexane (10/90). Fractions containing the required product were combined and evaporated to give tert-butyl (3-bromo-2-fluorophenyl) carbamate as a white solid (330mg)
With diphenyl phosphoryl azide; triethylamine; In toluene; at 100℃; for 2h; To 3-bromo-2-fluorobenzoicacid (10.0 g, 45.7 mmol) in 100 mL of toluene, were added by Et3N(7.7 mL, 54.8 mmol) and DPPA (15.0 g, 54.8 mmol). The mixture was heated to 1000C. When gas evolved, t-BuOH(10 mL) was added and stirring was kept for additional 2 hours. The mixture was cooled down and washedsuccessively by saturated Na2CO3 solution, 10% citric acidand brine. The organic layer was collected, dried over Na2SO4and concentrated to get the N-Bocprotected intermediate, which was used directly for next step.The crudesuspended in 30 mL of DCM, was added by TFA (15 mL). The mixture was thenstirred at rt for 2 hours. The resulting solid was filtered off and 5 M ofHCl/MeOH was added to the filtrate, forming the yellow solid, which wascollected and neutralized by saturated Na2CO3 solution toget free base as brown oil. (6.5 g, 71% yield)
To <strong>[161957-56-8]3-bromo-2-fluorobenzoic acid</strong> (10.0 g, 45.7 mmol) in 100 mL of toluene, were added by Et3N (7.7 mL, 54.8 mmol) and DPPA (15.0 g, 54.8 mmol). The mixture was heated to 100 C. When gas evolved, t-BuOH (10 mL) was added and stirring was kept for additional 2 hours. The mixture was cooled down and washed successively by saturated Na2CO3 solution, 10% citric acid and brine. The organic layer was collected, dried over Na2SO4 and concentrated to get the N-Boc protected intermediate, which was used directly for next step.

 

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