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[ CAS No. 20357-70-4 ] {[proInfo.proName]}

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Chemical Structure| 20357-70-4
Chemical Structure| 20357-70-4
Structure of 20357-70-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 20357-70-4 ]

CAS No. :20357-70-4 MDL No. :MFCD00012313
Formula : C13H10O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 198.22 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 20357-70-4 ]

* 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 [ 20357-70-4 ]

[ 20357-70-4 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 20357-70-4 ]
  • [ 86-77-1 ]
YieldReaction ConditionsOperation in experiment
98% With L-Selectride In tetrahydrofuran at 67℃; for 48h;
95% With 1-n-butyl-3-methylimidazolim bromide; toluene-4-sulfonic acid; 1-butyl-3-methylimidazolium Tetrafluoroborate at 115℃; for 10h;
  • 2
  • [ 18113-03-6 ]
  • [ 20357-70-4 ]
  • 3
  • [ 20357-70-4 ]
  • [ 5834-17-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: aqueous nitric acid; acetic acid 2: aqueous hydrochloric acid; tin (II)-chloride
Multi-step reaction with 2 steps 1: aqueous nitric acid; chlorobenzene 2: Raney nickel; ethanol / Hydrogenation.unter Druck
  • 4
  • [ 86-77-1 ]
  • [ 74-88-4 ]
  • [ 20357-70-4 ]
YieldReaction ConditionsOperation in experiment
100% With sodium hydride In tetrahydrofuran at 0 - 20℃; for 1h; Preparation of 2-methoxydibenzo[b,d]furan (3) To a solution of compound 2 (1.84 g, 0.01 mol) in dry THF, NaH (0.28 g,0.012 mol) was added at 0°C. After stirring the reaction mixture for 10 min, ICH3 (1.70 g, 0.012 mol) was added and stirring was continued at RT for 1 h. After completion of the reaction (monitored by TLC), the mixture was carefully quenched with water and extracted with CH2Cl2 (2 x 50 mL). The combined organic layerswere dried with Na2SO4 and the solvent was evaporated under reduced pressure. Chromatographic purification of the crude reaction mixture (on silica gel using 90:10, hexane:CH2Cl2 as eluent) gave 3 in quantitative yield as a yellow liquid which upon standing at -10°C turned into a white solid. 1H NMR (CDCl3, 400 MHz): δ 7.92 (d, J = 7.0 Hz, 1H), 7.55 (d, J = 8.3 Hz,1H), 7.49-7.41 (multiple peaks, 3H), 7.33 (td, J = 7.3 and 0.7 Hz, 1H), 7.05 (dd,J = 9.0 and 2.6 Hz, 1H), 3.92 (s, 3H).
  • 5
  • [ 84594-95-6 ]
  • [ 20357-70-4 ]
YieldReaction ConditionsOperation in experiment
89% With potassium phosphate; dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; palladium(II) acetylacetonate In toluene at 150 - 160℃; for 24h; Inert atmosphere; Sealed tube;
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