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Chemical Structure| 84102-78-3 Chemical Structure| 84102-78-3

Structure of 84102-78-3

Chemical Structure| 84102-78-3

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Product Details of [ 84102-78-3 ]

CAS No. :84102-78-3
Formula : C10H7NO2
M.W : 173.17
SMILES Code : N#CC1=CC=C(OC(CO)=C2)C2=C1

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Application In Synthesis of [ 84102-78-3 ]

* 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 [ 84102-78-3 ]

[ 84102-78-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2296-23-3 ]
  • [ 107-19-7 ]
  • [ 84102-78-3 ]
YieldReaction ConditionsOperation in experiment
67% With pyridine; copper(I) oxide; for 0.75h;Inert atmosphere of N2; Reflux; Propargyl alcohol (0.24 ml; 5.2 mmol) was added drop wise during 30 min to a refluxed suspension of the product of Step A (0.48 g; 1.96 mmol) and Cu2O (0.28 g; 1 .96 mmol) in anhydrous pyridine ( 4 ml) with stirring under N2. After additional reflux for 15 min, the mixture was cooled to room temperature, diluted to 20 ml with ethyl acetate (EtOAc) and insoluble material was removed by filtration. The filtrate was evaporated to dryness under reduced pressure and the residue was diluted to 20 ml with EtOAc, washed with diluted HCI (10 ml). The insoluble material formed was filtered off and the organic phase was washed with H2O (5 ml), brine, dried over anhydrous MgSO4, filtered and the filtrate evaporated to dryness. The residue was purified by flash column chromatography (FCC) (SiO2, CH2CI2 and EtOAc, 9 : 1 ) to give the title compound (0.23 g; 67%) as a colourless solid. 1H- NMR (CDCI3) 7.86 (m, 1 H); 7.49 - 7.55 (m, 2H); 6.72 (d, 1 H, J = 3 Hz); 4.8 (d, 2H, J = 3 Hz); 2.18 (broad s, 1 H);
67% With pyridine; copper(I) oxide; for 0.75h;Inert atmosphere; Reflux; Propargyl alcohol (0.24 ml; 5.2 mmol) was added drop wise during 30 min to a refluxed suspension of the product of Step A (0.48 g; 1 .96 mmol) and Cu20 (0.28 g; 1 .96 mmol) in anhydrous pyridine ( 4 ml) with stirring under N2. After additional reflux for 15 min, the mixture was cooled to room temperature, diluted to 20 ml with ethyl acetate (EtOAc) and insoluble material was removed by filtration. The filtrate was evaporated to dryness under reduced pressure and the residue was diluted to 20 ml with EtOAc, washed with diluted HCI (10 ml). The insoluble material formed was filtered off and the organic phase was washed with H20 (5 ml), brine, dried over anhydrous MgS04, filtered and the filtrate evaporated to dryness. The residue was purified by flash column chromatography (FCC) (Si02, CH2CI2 and EtOAc, 9 : 1 ) to give the title compound (0.23 g; 67%) as a colourless solid. 1 H-NMR (CDCI3) 7.86 (m, 1 H); 7.49 - 7.55 (m, 2H); 6.72 (d, 1 H, J = 3 Hz) ; 4.8 (d, 2H, J = 3 Hz) ; 2.18 (broad s, 1 H);
 

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