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Chemical Structure| 87755-82-6 Chemical Structure| 87755-82-6

Structure of 87755-82-6

Chemical Structure| 87755-82-6

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Product Details of [ 87755-82-6 ]

CAS No. :87755-82-6
Formula : C20H17NO2
M.W : 303.35
SMILES Code : O=CC1=CC=C(N(C2=CC=C(OC)C=C2)C3=CC=CC=C3)C=C1

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Application In Synthesis of [ 87755-82-6 ]

* 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 [ 87755-82-6 ]

[ 87755-82-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4316-51-2 ]
  • [ 68-12-2 ]
  • [ 87755-82-6 ]
YieldReaction ConditionsOperation in experiment
94.8% With trichlorophosphate; at 0 - 80℃; for 1h;Inert atmosphere; To a 250 mL four-necked flask was added a solution of 4-methoxytriphenylamine in DMF (previously prepared from 5.5 g of 4-methoxytriphenylamine dissolved in 75 mL of DMF), protected by nitrogen and magnetically stirred and cooled to 0 C. ,Using a constant pressure dropping funnel, 12.24g of POCl3 was slowly added dropwise to the reaction solution. After the addition was completed, the reaction conditions were maintained for 1h. Heating to 80 reaction.After the reaction was completed, the reaction mixture was poured into ice water and quenched, extracted with methylene chloride, washed with deionized water five times and anhydrous sulfurThe mixture was dried over magnesium sulfate, filtered and concentrated under reduced pressure to remove the solvent. The crude product was separated by column chromatography (petroleum ether / ethyl acetate = 10/1, v / v)Pure, to obtain a green oily liquid, the yield was 94.8%.
69% With trichlorophosphate; In 1,2-dichloro-ethane; for 4h;Reflux; POCl3 (6 mL, 64.17 mmol) was carefully added to a solution of 4-methoxy-N,N-diphenylaniline (10 g, 36.32 mmol), DMF (5 mL, 64.85 mmol) and 50 mL of 1,2-dichloroethane. The mixture was refluxed for 4 h, then cooled to room temperature (r.t.), and poured into a saturated aqueous sodium acetate solution (100 mL). The product was extracted with dichloromethane. The organic layer was dried over anhydrous MgSO4. The solvent was evaporated by a rotary evaporator. The residue was purified by silica gel column chromatography using ethyl acetate: n-hexane (2:3) to give (1) (7.6 g, Yield: 69%). TOF/MS (ESI): found 326.1 (M+Na+). 1H NMR (300 MHz, CDCl3, delta): 9.79 (s, 1H, ArCHO), 7.68-6.89 (m, 14H, ArH), 3.83 (s, 3H, ArOCH3).
 

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