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[ CAS No. 951667-98-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 951667-98-4
Chemical Structure| 951667-98-4
Structure of 951667-98-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 951667-98-4 ]

CAS No. :951667-98-4 MDL No. :MFCD16744200
Formula : C9H11FN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 198.19 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 951667-98-4 ]

* 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 [ 951667-98-4 ]

[ 951667-98-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 700-36-7 ]
  • [ 109-73-9 ]
  • [ 951667-98-4 ]
YieldReaction ConditionsOperation in experiment
At RT and under nitrogen, Pd(OAc)2 (24 mg, 0.11 mmol) and BINAP (74 mg, 0.12 mmol) were added to a solution of butylamine (173 mg, 2.37 mmol) and 4-fluoro-2-bromonitrobenzene (460 mg, 2.09 mmol) in toluene (3 mL, degassed bu purging). The reaction mixture was heated at 100 C. for 3 minutes and then cooled to 0 C. NaOtBu (271 mg, 2.82 mmol) was added and immediately the reaction mixture turned red. The reaction was stirred at 70 C. for 16 h. The reaction was cooled to RT and filtered over Kiezelguhr. The residue was rinsed with EtOAc (30 mL). The EtOAc-layer was washed with brine (30 mL). The aqueous-layer was extracted once more with EtOAc (30 mL). The combined EtOAc-extracts were dried (Na2SO4), filtered, and evaporated to drynessin vacuo. The crude product was purified by flash column chromatography (EtOAc/heptane: 1/100 to 1/30) to afford (5-fluoro-2-nitro-phenyl)-propyl-amine as a yellow oil (333 mg, 75%, purity (GC)=85%).MS: [M]+=212.
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