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Chemical Structure| 32766-61-3 Chemical Structure| 32766-61-3

Structure of 32766-61-3

Chemical Structure| 32766-61-3

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Product Details of [ 32766-61-3 ]

CAS No. :32766-61-3
Formula : C10H10O4
M.W : 194.18
SMILES Code : O=C(C(C1=CC=C(OC)C=C1)=O)OC
MDL No. :MFCD00101050

Safety of [ 32766-61-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 32766-61-3 ]

* 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 [ 32766-61-3 ]

[ 32766-61-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 32766-61-3 ]
  • [ 70298-89-4 ]
  • 3-hydroxy-3-(4-methoxyphenyl)-1,3-dihydro-2H-pyrrolo[3,2-c]pyridin-2-one [ No CAS ]
  • 2
  • [ 32766-61-3 ]
  • [ 70298-89-4 ]
  • methyl 2-{4-[(2,2-dimethyl-1-oxopropyl)amino]pyridin-3-yl}-2-hydroxy-2-(4-methoxyphenyl)-acetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% General procedure: To a stirred solution of 1a (0.36 g, 2.0mmol) in THF (5 mL) at ?78 C was added n-BuLi (1.6 M in hexane; 4.0 mmol) dropwise. After 15 min,temperature was raised to 0 C and stirring was continued for 2.5 h. Then, the mixture was cooled to ?78C and MeCOCO2Me (0.20 g, 2.0 mmol) was added dropwise. The resulting mixture was graduallywarmed to 0 C, treated with saturated aqueous NH4Cl (20 mL), and extracted with AcOEt (3 × 15 mL).The combined extracts were washed with brine (15 mL), dried (Na2SO4), and concentrated by evaporation.The residue was purified by column chromatography on SiO2 (AcOEt/hexane 1:3) to afford 2a (0.28 g,50percent);
 

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