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Chemical Structure| 60751-75-9 Chemical Structure| 60751-75-9

Structure of 60751-75-9

Chemical Structure| 60751-75-9

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Product Details of [ 60751-75-9 ]

CAS No. :60751-75-9
Formula : C9H10INO
M.W : 275.09
SMILES Code : CCC(NC1=CC=CC=C1I)=O
English Name :N-(2-Iodophenyl)propionamide

Safety of [ 60751-75-9 ]

Application In Synthesis of [ 60751-75-9 ]

* 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 [ 60751-75-9 ]

[ 60751-75-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 60751-75-9 ]
  • [ 6797-13-3 ]
YieldReaction ConditionsOperation in experiment
48% With caesium carbonate In N,N-dimethyl-formamide at 140℃; for 24h; Green chemistry; 5. General procedure for the synthesis of benzoxazole General procedure: To a dried sealed tube, 2-haloanilide (1eq.), en-PAN-Cu catalyst (10 mol %), CS2CO3 (2 eq.) were added followed by the addition of DMF (2ml). The reaction was stirred at 140°C for 24h. The progress of the reaction was monitored by TLC. After the completion of the reaction, catalyst was filtered and the filtrate was extracted with ethyl acetate and brine. The organic layer was separated and dried over sodium sulphate and concentrated on rotary evaporator. The crude product thus obtained was purified by column chromatography on silica gel using hexane/ethyl acetate as eluent. The products were confirmed by 1H NMR, 13C NMR, IR and GC-MS analyses.
38% With [2,2]bipyridinyl; copper(l) iodide; caesium carbonate In N,N-dimethyl-formamide at 140℃; for 16h; Sealed tube; Molecular sieve; General procedure for the synthesis of benzoxazole 4 General procedure: To a dried sealed tube, 2-haloanilide (0.6 mmol), CuI (0.03 mmol), 2,2’-bipyridine (0.06 mmol), Cs2CO3 (2equiv.) were added followed by DMF (4ml)and 4 Å molecular sieves ( 0.1g).The reaction mixture was then stirred at 140 °C for 16 h under air atmosphere and the progress of the reaction was monitored by TLC. On completion of the reaction, the reaction mixture was diluted with ethyl acetate, filtered through celite pad. The diluted solution was then extracted with ethyl acetate (10 x 3 ml) and brine solution. The organic layer was separated and dried over anhydrous Na2SO4, and concentrated on a vacuum rotary evaporator. The resulting crude product was purified by column chromatography on silica gel using n-hexane/ethyl acetate as eluent to afford the pure product. The products were confirmed by 1H NMR, 13CNMR, IR and HRMS analysis.
35% With 1-(N-ferrocenylmethyl)benzimidazole grafted onto Merrifield resin In dimethyl sulfoxide at 140℃; for 23h; 4.4. General procedure for the synthesis of 2-substituted benzoxazoles General procedure: A mixture of N-(2-iodoaryl)benzamides/acetamide/propanamide (1 mmol) and [FemMerBenz]OH (100 mg, 0.12 mmol) in dry DMSO (5 mL) was stirred for 15-24 h at 140 C. The reaction mixture was filtered and quenched withwater (10 mL). The resultant solutionwas extracted with ethyl acetate (3*10 mL). The combined organic layers were dried over Na2SO4. The solventwas evaporated in vacuo to give the crude product, which was purified by column chromatography over silica gel using hexane/EtOAc as the eluent.
 

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