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Chemical Structure| 1132940-78-3 Chemical Structure| 1132940-78-3

Structure of 1132940-78-3

Chemical Structure| 1132940-78-3

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Product Details of [ 1132940-78-3 ]

CAS No. :1132940-78-3
Formula : C18H14BrNO2
M.W : 356.21
SMILES Code : O=C(OCC1=CC=CC=C1)NC2=CC=C3C=C(Br)C=CC3=C2
MDL No. :MFCD31628732

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Application In Synthesis of [ 1132940-78-3 ]

* 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 [ 1132940-78-3 ]

[ 1132940-78-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7499-66-3 ]
  • [ 501-53-1 ]
  • [ 1132940-78-3 ]
YieldReaction ConditionsOperation in experiment
52% With sodium hydrogencarbonate; In water; acetone; at 0 - 20℃; for 19h; Part C. Preparation of benzyl 6-bromonaphthalen-2-ylcarbamate.; [00750] A mixture of the product from Part B (1.79g, 8.06mmol) and saturated sodium bicarbonate solution (18mL) in acetone (4OmL) at 0 0C was treated drop wise with benzyl chloroformate. The mixture was stirred at 00C for Ih, and then allowed to gradually warm to room temperature over 18h. The mixture was diluted with EtOAc and water and the layers separated. The organic layer was extracted with water and washed with brine. Dried over Na2SO^ filtered and concentrated under vacuum. Purification by silica gel column chromatography eluting with EtOAc/hexanes gave the title compound as a pink solid (1.5g, 52percent).
52% With sodium hydrogencarbonate; In water; acetone; at 0 - 20℃; for 19h; Part C. Preparation of benzyl 6-bromonaphthalen-2-ylcarbamate.; [00493] A mixture of the product from Part B (1.79g, 8.06mmol) and saturated sodium bicarbonate solution (18mL) in acetone (4OmL) at 0 0C was treated drop wise with benzyl chloroformate. The mixture was stirred at O0C for Ih, and then allowed to gradually warm to room temperature over 18h. The mixture was diluted with EtOAc and water and the layers separated. The organic layer was extracted with water and washed with brine. Dried over Na2SO4, filtered and concentrated under vacuum. Purification by silica gel column chromatography eluting with EtOAc/hexanes gave the title compound as a pink solid (1.5g, 52percent).
 

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