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Chemical Structure| 53623-81-7 Chemical Structure| 53623-81-7

Structure of 53623-81-7

Chemical Structure| 53623-81-7

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Product Details of [ 53623-81-7 ]

CAS No. :53623-81-7
Formula : C9H12N2O
M.W : 164.20
SMILES Code : N=C(N)C1=CC=CC=C1OCC
MDL No. :MFCD05663104

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Application In Synthesis of [ 53623-81-7 ]

* 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 [ 53623-81-7 ]

[ 53623-81-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6609-57-0 ]
  • [ 53623-81-7 ]
YieldReaction ConditionsOperation in experiment
89% With hydroxylamine hydrochloride; triethylamine; In ethanol; for 4h;Reflux; 150 mL of ethanol, 4.14 g (0.06 mol) of hydroxylamine hydrochloride and 6 g (0.06 mol) of triethylamine were placed in a 250 mL three-necked flask, and heated to 50-60 C for 1 h.After 1 h, 7.2 g of compound VII was added to the flask, and the reaction was refluxed for 4 h.The compound VII disappeared by TLC, and ethanol was removed by rotary evaporation. 150 mL of water was added to the flask to dissolve the triethylamine hydrochloride, and the residue was filtered and filtered.The cake was Compound VIII, and after drying, it was obtained as a white solid, 9.61 g, yield 89%.
With trimethylaluminum; ammonium chloride; In toluene; at 0 - 80℃; for 7h; To a solution of <strong>[6609-57-0]2-ethoxybenzonitrile</strong> (2, 10 g, 68 mmol) in toluene (150 mL) was added AICH3CINH2 (1 eq). The methylchloroaluminum amide was freshly prepared, in-situ; NH4CI (0.535 g, 10 mmol) was dissolved in dry toluene (10 mL) at 000 and trimethylaluminum (2 M in toluene, 5.0 mL, 10 mmol) was added and the reaction was warmed to r.t. and stirred for 1 hour to give theAICH3CINH2, which was used directly. The mixture was stirred at 80 00 for 6 hours. The reaction mixture was concentrated under vacuo to give crude I24a (8.42 g, 75.4% yield). ESI-MS (Mi-i): 165 calc. for 09H12N20: 164.2.
With amino(methyl)aluminum chloride; In toluene; at 80℃; for 6h; Preparation of intermediate l-34a: 2-Ethoxybenzamidine To a solution of <strong>[6609-57-0]2-ethoxybenzonitrile</strong> (2, 10 g, 68 mmol) in toluene (150 ml_) was added AICH3CINH2 (1 eq). The methylchloroaluminum amide was freshly prepared, in-situ; NH4CI (0.535 g, 10 mmol) was dissolved in dry toluene (10 ml_) at 0 C and trimethylaluminum (2 M in toluene, 5.0 ml_, 10 mmol) was added and the reaction was warmed to r.t. and stirred for 1 hour to give the AICH3CINH2, which was used directly. The mixture was stirred at 80 C for 6 hours. The reaction mixture was concentrated under vacuo to give crude l-34a (8.42 g, 75.4% yield). ESI-MS (M+1 ): 165 calc. for C9H12N2O: 164.2.
 

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