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Chemical Structure| 59114-88-4 Chemical Structure| 59114-88-4

Structure of 59114-88-4

Chemical Structure| 59114-88-4

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Product Details of [ 59114-88-4 ]

CAS No. :59114-88-4
Formula : C11H11BrO2
M.W : 255.11
SMILES Code : O=C(OCC)/C=C/C1=CC=CC(Br)=C1
MDL No. :MFCD11111008

Safety of [ 59114-88-4 ]

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 [ 59114-88-4 ]

* 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.

  • Downstream synthetic route of [ 59114-88-4 ]

[ 59114-88-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-04-7 ]
  • [ 59114-88-4 ]
  • [ 58473-74-8 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate;silica gel; In methanol; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; Trans ethyl 3-bromocinnamate (8.4 g), ethylamine (6.7 g), methanol (18 ml) and 4A molecular sieves (1 g) were combined and heated at reflux for 1/2 hour. The mixture was cooled to about 45 C. and sodium methylate (0.6 g) added. The mixture was then heated at reflux 11/2 hour and then cooled. It was acidified with concentrated hydrochloric acid (12 ml). The sieves were removed by filtration. Ice water was added to the filtrate to precipitate trans 3-bromo-N-ethylcinnamamide, m.p. 89-90 C. (after recrystallization from ethanol/water).
 

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