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Chemical Structure| 141798-56-3 Chemical Structure| 141798-56-3

Structure of 141798-56-3

Chemical Structure| 141798-56-3

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Product Details of [ 141798-56-3 ]

CAS No. :141798-56-3
Formula : C12H12N2O
M.W : 200.23
SMILES Code : OC1=CC=C(NC2=CC=CC=C2N)C=C1
Boiling Point : No data available

Safety of [ 141798-56-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-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 [ 141798-56-3 ]

* 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 [ 141798-56-3 ]

[ 141798-56-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2082-59-9 ]
  • [ 54381-08-7 ]
  • [ 141798-56-3 ]
  • [ 123-30-8 ]
  • [ 88-73-3 ]
  • 2-Butyl-3-(4-hydroxyphenyl)benzimidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride;palladium-carbon; In methanol; dimethyl sulfoxide; ethyl acetate; Preparation 14 2-Butyl-3-(4-hydroxyphenyl)benzimidazole A mixture of (8.0 g, 51 mmol, 1.0 eq) 1-chloro-2-nitrobenzene and (5.54 g, 51 mmol, 1.0 eq) 4-aminophenol in 40 ml of dry dimethylsulfoxide was heated to reflux for 18 hours. The reaction mixture was cooled, poured into 400 ml of 0.1N HCl and 400 ml ethyl acetate, stirred, and filtered through celite. The filtrate layers were separated, and the aqueous layer was extracted with ethyl acetate. The ethyl acetate extracts were combined, washed twice with H2O, once with brine, dried over MgSO4, and concentrated to give 8 g of a dark oil. Silica gel chromatography eluding with 20% ethyl acetate/hexane gave 1.63 g, 14%, of a red solid. A mixture of (1.6 g, 6.89 mmol, 1.0 eq) <strong>[54381-08-7]4-N-(2-nitrophenyl)amino phenol</strong> and 800 mg of 10% Pd/C in 100 ml ethyl acetate was placed on a Parr hydrogenation apparatus and shaken under 50 psi H2 for 3 hours. The mixture was filtered through celite, concentrated in vacuo , and chromatographed on a silica gel column eluding with 50% ethyl acetate/hexane to give 1.3 g, 94%, of an orange-yellow solid. A mixture of (600 mg, 3.00 mmol, 1.0 eq) 4-N-(2-aminophenyl)amino phenol and 10 ml valeric anhydride was heated to reflux for 18 hours. The mixture was taken up in 50 ml of methanol, basified with 2N NaOH to pH 10, and stirred 1 hour at room temperature. The reaction mixture was then neutralized and extracted twice with ethyl acetate. The ethyl acetate extracts were combined, washed twice with H2O, once with brine, dried over MgSO4 and concentrated to give 1 g of an oil. Silica gel chromatography eluding with 21/2% CH3OH-CH2Cl2 gave 124 mg, 16%, solid. M.P.: 192-194C.
 

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