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1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide

Base Information Edit
  • Chemical Name:1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide
  • CAS No.:496067-62-0
  • Molecular Formula:C24H36N3O*I
  • Molecular Weight:509.474
  • Hs Code.:
  • Mol file:496067-62-0.mol
1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide

Synonyms:1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide

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Chemical Property of 1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide Edit
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Technology Process of 1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide

There total 6 articles about 1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide 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 5 steps
1: 95 percent / Et3N / CH2Cl2 / 12 h / 25 °C
2: 60 percent / NaBH4 / ethanol / 12 h / 25 °C
3: 80 percent / Et3N / CH2Cl2 / 24 h / 0 - 25 °C
4: 89 percent / KI / acetone / 4 h / 56 °C
5: dimethylformamide / 12 h / 80 °C
With sodium tetrahydroborate; triethylamine; potassium iodide; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja028142b
Guidance literature:
Multi-step reaction with 2 steps
1.1: H3PO4 / H2O; dioxane / 0.5 h / 80 °C / pH 2
1.2: 36 percent / aq. NH4Cl / H2O; dioxane / 3 h / 100 °C
2.1: dimethylformamide / 12 h / 80 °C
With phosphoric acid; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/ja028142b
Guidance literature:
Multi-step reaction with 3 steps
1: 80 percent / Et3N / CH2Cl2 / 24 h / 0 - 25 °C
2: 89 percent / KI / acetone / 4 h / 56 °C
3: dimethylformamide / 12 h / 80 °C
With triethylamine; potassium iodide; In dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja028142b
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