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2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.05,9.06,10>dodec-11-en-7-one ethylene acetal

Base Information
  • Chemical Name:2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.05,9.06,10>dodec-11-en-7-one ethylene acetal
  • CAS No.:108418-64-0
  • Molecular Formula:C19H21N3O3
  • Molecular Weight:339.394
  • Hs Code.:
2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.0<sup>5,9</sup>.0<sup>6,10</sup>>dodec-11-en-7-one ethylene acetal

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Chemical Property of 2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.05,9.06,10>dodec-11-en-7-one ethylene acetal
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Technology Process of 2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.05,9.06,10>dodec-11-en-7-one ethylene acetal

There total 13 articles about 2-(N-phenylcarbamoyl)-2,3-diazatetracyclo<6.2.2.05,9.06,10>dodec-11-en-7-one ethylene acetal which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / CH2Cl2 / 3 h / Ambient temperature
2: 80 percent / KOH / H2O; dimethylsulfoxide / 3 h / 50 °C
With potassium hydroxide; In dichloromethane; water; dimethyl sulfoxide;
DOI:10.1021/jo00389a003
Guidance literature:
Multi-step reaction with 12 steps
1: 61 percent / 80percent m-chloroperoxybenzoic acid, sodium hydrogencarbonate / CH2Cl2 / 40 h / Ambient temperature
2: 1.) diphenyl diselenide, NaBH4, 2.) 30percent H2O2 / 1.) n-BuOH, reflux , 20 h, 2.) n-BuOH, THF, 16 h
3: 50 percent / chromium trioxide / pyridine; CH2Cl2 / 36 h / Ambient temperature
4: 85 percent / acetonitrile / 14 h / 0 °C / Irradiation
5: 95 percent / sodium borohydride / ethanol / 12 h
6: 79 percent / pyridine / 120 h / 5 °C
7: 65 percent / 1.5-diazabicyclo<4.3.0>non-5-ene / acetonitrile / 15 h / 80 °C
8: 90 percent / p-toluenesulfonic acid monohydrate / H2O; acetone / 0.33 h / Ambient temperature
9: 91 percent / lithium aluminium hydride / diethyl ether / 3 h / Heating
10: 85 percent / methyltriphenoxyphosphonium iodide / hexamethylphosphoric acid triamide / 5 h / 95 °C
11: 85 percent / CH2Cl2 / 3 h / Ambient temperature
12: 80 percent / KOH / H2O; dimethylsulfoxide / 3 h / 50 °C
With chromium(VI) oxide; potassium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; diphenyl diselenide; DBN; methyltriphenoxyphosphonium iodide; dihydrogen peroxide; sodium hydrogencarbonate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide; acetone; acetonitrile;
DOI:10.1021/jo00389a003
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