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Chemical Structure| 75152-19-1 Chemical Structure| 75152-19-1

Structure of 75152-19-1

Chemical Structure| 75152-19-1

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Product Details of [ 75152-19-1 ]

CAS No. :75152-19-1
Formula : C10H9NO3
M.W : 191.18
SMILES Code : O=C1CN=C(C2=CC=C(OC)C=C2)O1

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Application In Synthesis of [ 75152-19-1 ]

* 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 [ 75152-19-1 ]

[ 75152-19-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13214-64-7 ]
  • [ 75152-19-1 ]
YieldReaction ConditionsOperation in experiment
With diisopropyl-carbodiimide; In dichloromethane; at 0℃; for 1h;Inert atmosphere; General procedure: A solution of 1 (0.5 mmol) in CH2Cl2 (5 mL) in a round-bottom flask (25 mL) was cooled with ice-water, and then DIC (0.55 mmol) was added by a syringe. After the resultant mixture was stirred at 0 °C for 1 h, CH2Cl2 was removed by sparging N2 followed by adding 3a (0.55 mmol) or 3b (0.6 mmol) and toluene (10 mL). After refluxing for 3 h, the reaction mixture was diluted with EtOAc (6 mL), passed through a silica gel column, and then evaporated. The product 5a or 5b was isolated from the residue by preparative TLC (silica gel, EtOAc/PE 1/2-1/1, v/v).
With acetic anhydride;Heating; General procedure: A mixture of benzoyl glycines 1a?1d (0.02 mol) and 75 cm3 acetic anhydride was gently heated until a clear solution 2a?2d was obtained. The resulting solution(A) was cooled in an ice bath before treating with a solution (B) of naphthalene diazonium chloride prepared as follows: 3.2 g 1-naphthylamine (0.02 mol) was mixed with 5 cm3 H2O and 6 cm3 conc. HCl. The mixture was cooled in an ice bath and an aqueous solution of 1.38 g NaNO2(0.02 mol) was introduced dropwise and the resulting mixture was stirred for further 30 min. Freshly prepared crude solution (A) was added dropwise in the presence of 1.64 g anhydrous sodium acetate (0.02 mol) and the stirring was continued for further 2 h at 0 C. The resulting crude precipitate was filtered, washed with water, and dried
 

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