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Chemical Structure| 75637-30-8 Chemical Structure| 75637-30-8

Structure of 75637-30-8

Chemical Structure| 75637-30-8

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Product Details of [ 75637-30-8 ]

CAS No. :75637-30-8
Formula : C16H15NO3
M.W : 269.30
SMILES Code : O=C(N)C1=CC(C(C)=O)=CC=C1OCC2=CC=CC=C2

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Application In Synthesis of [ 75637-30-8 ]

* 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 [ 75637-30-8 ]

[ 75637-30-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 40187-51-7 ]
  • [ 100-44-7 ]
  • [ 75637-30-8 ]
  • 2
  • [ 40187-51-7 ]
  • [ 100-39-0 ]
  • [ 75637-30-8 ]
YieldReaction ConditionsOperation in experiment
98% With potassium carbonate; In acetonitrile;Reflux; 5-Acetyl-2-hydroxybenzamide (8.2g, 45.76 mmol), K2C03 (9.488g, 68.65 mmol, 1 .5 eq) and BnBr (8.609g, 5.987 mL, 50.34 mmol, 1 .1 eq) were heated under reflux in eCN (100 mL) overnight. The mixture remained a white suspension throughout. After removal of MeCN under reduced pressure, the crude product was dispersed in water (100 mL), and extraction with EtOAc (50 mL) was attempted. The white precipitate was found to be insoluble in either layer, and so was collected by filtration (vacuum) to give 9.41 g of white solid. The aqueous layer was separated in the filtrate and washed with EtOAc (50 mL). Concentration of the combined organic layers gave a white solid with an odour of BnBr. This was sonicated in PE, before filtering, and washing with a small amount of DCIWPE (1 :1 ). Total recovered yield of product: 12.077 g (98%).
98% With potassium carbonate; In acetonitrile;Reflux; 5-Acetyl-2-hydroxybenzamide (4.1 ) (8.2g, 45.76 mmol), K2C03 (9.488g, 68.65 mmol, 1 .5 eq) and BnBr (8.609g, 5.987 mL, 50.34 mmol, 1 .1 eq) were heated under reflux in MeCN (100 mL) overnight. The mixture remained a white suspension throughout. After removal of MeCN under reduced pressure, the crude product was dispersed in water (100 mL), and extraction with EtOAc (50 mL) was attempted. The white precipitate was found to be insoluble in either layer, and so was collected by filtration (vacuum) to give 9.41 g of white solid. The aqueous layer was separated in the filtrate and washed with a further 50 mL of EtOAc. Concentration of the combined organic layers gave a white solid with an odour of BnBr. This was sonicated in PE, before filtering, and washing with a small amount of DCM/PE 1 :1 . The total recovered yield of product (4.2) is 12.077g (98%)
 

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