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[ CAS No. 4383-22-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 4383-22-6
Chemical Structure| 4383-22-6
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Product Details of [ 4383-22-6 ]

CAS No. :4383-22-6 MDL No. :MFCD00463446
Formula : C10H13N Boiling Point : -
Linear Structure Formula :CH2CHCH2NH(CH2C6H5) InChI Key :RHUCQDQRNUUMKY-UHFFFAOYSA-N
M.W : 147.22 Pubchem ID :521150
Synonyms :

Safety of [ 4383-22-6 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3267
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4383-22-6 ]

* 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 [ 4383-22-6 ]

[ 4383-22-6 ] Synthesis Path-Downstream   1~4

  • 3
  • [ 4383-22-6 ]
  • [ 111771-08-5 ]
  • [ 1050203-43-4 ]
YieldReaction ConditionsOperation in experiment
67% A mixture of <strong>[111771-08-5]2-fluoro-6-iodobenzoic acid</strong> (Intermediate A, 30 g, 112.78 mmol) in SOCl2 (60 mL) was heated at 800C for 1.5 h. Excess SOCl2 was removed in vacuo and the residue obtained was added to a solution of triethylamine (13.7 g, 135.64 mmol) in THF (50 mL). This solution was added dropwise to a solution of N-benzylprop-2-en- 1-amine (Intermediate B,16.6 g, 112.93 mmol) in THF (15OmL) cooled to 5C. The resulting solution stirred at RT for 2 h. The mixture was concentrated and the residue was dissolved in EtOAc (200 mL). The organic layer was washed with aqueous NaHSO4 (2x50 mL), aqueous NaHCO3 (1x50 mL), and brine (1x50 mL), dried over Na2SO4, and evaporated to dryness to afford 30.0 g (67%) of N-allyl-N-benzyl-2- fluoro-6-iodobenzamide as a white solid.
  • 4
  • [ 4383-22-6 ]
  • [ 51307-59-6 ]
  • [ 1401332-25-9 ]
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