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Chemical Structure| 84827-47-4 Chemical Structure| 84827-47-4

Structure of 84827-47-4

Chemical Structure| 84827-47-4

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Product Details of [ 84827-47-4 ]

CAS No. :84827-47-4
Formula : C13H19NO2
M.W : 221.30
SMILES Code : O=C(OC(C)(C)C)CNC1=CC=C(C)C=C1

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Application In Synthesis of [ 84827-47-4 ]

* 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 [ 84827-47-4 ]

[ 84827-47-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 932-32-1 ]
  • [ 84827-47-4 ]
  • C20H25ClN2O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
53% With methylene blue; In acetonitrile; at 50℃; for 24h;Irradiation; General procedure: A suspension of N-arylglycine ester 1 (0.5 mmol), N-substituted anilines 2 (0.6 mmol) and Methylene blue (0.025 mmol) in CH3CN was stirred for 24 h at 50 C under an air atmosphere irradiated by blue lights. After cooling, water (10 mL) was added and the mixture was extracted with CH2Cl2 (3 x 10 mL). The combined organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residues were purified by flash column chromatography (n-hexane-EtOAc) to afford the desired product 3.
49% With methylene blue; In acetonitrile; at 45℃; for 18h;Irradiation; Green chemistry; tert-Butyl 2-(p-toluidine)acetate (0.5 mmol, 110.6 mg),<strong>[932-32-1]N-methyl-o-chloroaniline</strong> (0.75 mmol, 105.8 mg),Methylene blue (0.05 mmol, 16 mg) was added to a 25 mL two-necked flask.Add acetonitrile (5 mL) as solvent and stir.Under the blue light emitted by a 3W LED lamp,The reaction was carried out in an air atmosphere at a temperature of 45 C for 18 h.After the reaction,Water and ethyl acetate are added to the reaction system.Extraction layering,Divided into water and organic layers,Drying with anhydrous sodium sulfate in the organic layer,The dried organic layer was concentrated by distillation under reduced pressure to give a yellow oil.The obtained yellow oil was separated and purified by column chromatography on silica gel.a mixture of petroleum ether and ethyl acetate in a volume ratio of 15:1 as an eluent,Collect the eluent and distill off the solvent.88.2 mg of a white solid product were obtained.The yield is 49%, that is, the target product is obtained, and its structural formula is:
 

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