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Chemical Structure| 35929-79-4 Chemical Structure| 35929-79-4

Structure of 35929-79-4

Chemical Structure| 35929-79-4

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Product Details of [ 35929-79-4 ]

CAS No. :35929-79-4
Formula : C19H22ClNO4
M.W : 363.84
SMILES Code : O=C(C1=C(C)NC(C)=C(C(OCC)=O)C1C2=CC=C(Cl)C=C2)OCC
MDL No. :MFCD00087104
Boiling Point : No data available

Safety of [ 35929-79-4 ]

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

Application In Synthesis of [ 35929-79-4 ]

* 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.

  • Upstream synthesis route of [ 35929-79-4 ]

[ 35929-79-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 35929-79-4 ]
  • [ 105-45-3 ]
  • [ 73257-49-5 ]
YieldReaction ConditionsOperation in experiment
91% With ammonium hydroxide In ethanol at 110℃; Flow reactor General procedure: Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate (4a). EtOH solution (3 mL) ofbenzaldehyde (0.67 M) mixed with ethyl acetoacetate (1.34 M) and the 25percent aqueous NH3 (3 mL) wererespectively transferred into gas-tight syringe 1 and syringe 2. The syringes were placed in a LongerLSP02-1B syringe pump which was set to deliver the reactants into the mixer at identical flow rate of 6.7μL/min. The reaction mixture was then allowed to flow through a stainless steel tube reactor which wasdipped in a 110 C oil bath. The output mixture was collected in a cooled sample vial. After reactioncompletion, rinsed the reactor with ethanol to collect all of the reactant solution and then concentratedunder vacuum. The residue was subjected to silica gel column chromatography with Pet-EA (5:1) aseluent to give 4a (612mg, 93percent yield).
References: [1] Heterocycles, 2016, vol. 93, # 2, p. 755 - 761.
 

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