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Chemical Structure| 106918-32-5 Chemical Structure| 106918-32-5

Structure of 106918-32-5

Chemical Structure| 106918-32-5

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Product Details of [ 106918-32-5 ]

CAS No. :106918-32-5
Formula : C10H10O3
M.W : 178.18
SMILES Code : O=C(OC)C1=CC=C(CC=O)C=C1
MDL No. :MFCD11846871
InChI Key :HKTGGDULWDLYKQ-UHFFFAOYSA-N
Pubchem ID :13844675

Safety of [ 106918-32-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 106918-32-5 ]

* 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 [ 106918-32-5 ]

[ 106918-32-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 106918-32-5 ]
  • [ 22744-12-3 ]
YieldReaction ConditionsOperation in experiment
28% With Jones reagent; In acetone; at -50 - -30℃; for 1h; To a solution of methyl 4-(2-methoxyethyl) benzoate (E9) (2.41 g, 12.5 mmol) in dioxane (50 ml) 1 N water solution of HCl (40 ml) was added and the resultant mixture was stirred at room temperature for 12 hours. The reaction mixture was extracted with ethyl acetate (3 x 50 ml), the organic extracts were combined, washed with brine (2 x 30 ml), and dried (Na2SO4). The solvents were evaporated, the residue was dissolved in acetone (70 ml) and cooled to -50C. To the cold solution at this temperature slowly (ca. for 5 minutes) 2.67 M Jones reagent (CrO3/H2S04 ; 7.5 ml, 20.0 mmol) was added and the obtained mixture was stirred at-40 to-50C for 1 hour and at-30C for 20 minutes. Isopropyl alcohol (2 ml) was added to the reaction mixture and the cooling bath was removed allowing the reaction to warm up for 10 minutes. The mixture was poured into water (150) and extracted with ethyl acetate (3 x 100 ml). The organic layers were combined, washed with brine (2 x 50), and dried (Na2SO4). The solvent was evaporated and the residue was dissolved in a small amount of hot dioxane (1-2 ml). Addition of petroleum ether (4-6 ml) caused the formation of a precipitate. The mixture was filtered and the precipitate was washed with dioxane-petroleum ether (1 : 4). The filtrate was evaporated and the precipitate formation procedure was repeated as described above. Then the filtrate was evaporated and the residue was chromatographed on silicagel (100 g) with petroleum ether-dioxane-acetic acid (2.5 : 7.5 : 0.1) to give the title compound (0.681 g, 28%) as a white solid. 1H NMR (CDCl3, HMDSO) delta: 3.68 (2H, s); 3.89 (3H, s); 7.33 (2H, d, J=8.2 Hz); 7.97 (2H, d, J=8.2 Hz); 10.82 (1H, br s).
  • 2
  • [ 106918-32-5 ]
  • [ 347174-05-4 ]
  • ethyl 4-(cyclohexylamino)-3-(4-(methoxycarbonyl)-benzylamino)benzoate [ No CAS ]
  • 3
  • [ 46112-46-3 ]
  • [ 106918-32-5 ]
 

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