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Chemical Structure| 1374150-50-1 Chemical Structure| 1374150-50-1

Structure of 1374150-50-1

Chemical Structure| 1374150-50-1

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Product Details of [ 1374150-50-1 ]

CAS No. :1374150-50-1
Formula : C8H4F2O3
M.W : 186.11
SMILES Code : O=C(O)C1=CC(F)=C(F)C=C1C=O
MDL No. :MFCD23161461

Safety of [ 1374150-50-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1374150-50-1 ]

* 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 [ 1374150-50-1 ]

[ 1374150-50-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 878207-28-4 ]
  • [ 68-12-2 ]
  • [ 1374150-50-1 ]
YieldReaction ConditionsOperation in experiment
A solution of R-14 (333 mg, 1.33 mmol) in anhydrous THF (5 mL) is cooled to -30 C and isopropyl magnesium chloride (2M in THF, 0.99 mL, 1.99 mmol) is added. The reaction is stirred at -30 C for 4 hours, DMF (1.03 mL, 13.27 mmol) is added and the mixture is warmed to room temperature and stirred for 1.5 hours. The reaction mixture is concentrated in vacuo and the residue acidified to pH 1 using 0.5M aqueous HCl. The product is extracted into CH2CI2 and the combined organics are washed with brine and then dried with Na2S04, filtered and concentrated in vacuo. The residue is purified by flash chromatography (Si02, 20-40% EtOAc in cyclohexane) to give R-16 (50.3 mg).
 

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