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2-(3-chlorophenyl)-7-azaspiro[3.5]nonane

Base Information Edit
  • Chemical Name:2-(3-chlorophenyl)-7-azaspiro[3.5]nonane
  • CAS No.:1225276-16-3
  • Molecular Formula:C14H18ClN
  • Molecular Weight:235.757
  • Hs Code.:
  • Mol file:1225276-16-3.mol
2-(3-chlorophenyl)-7-azaspiro[3.5]nonane

Synonyms:2-(3-chlorophenyl)-7-azaspiro[3.5]nonane

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Chemical Property of 2-(3-chlorophenyl)-7-azaspiro[3.5]nonane Edit
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Technology Process of 2-(3-chlorophenyl)-7-azaspiro[3.5]nonane

There total 5 articles about 2-(3-chlorophenyl)-7-azaspiro[3.5]nonane 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:
tert-butyl 2-(3-chlorophenyl)-2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate; With triethylsilane; boron trifluoride diethyl etherate; trifluoroacetic acid; In dichloromethane; at 0 ℃; for 1h;
With sodium hydrogencarbonate; In ethyl acetate;
Guidance literature:
Multi-step reaction with 3 steps
1: carbon tetrabromide; triphenylphosphine / tetrahydrofuran
2: nickel(II) iodide; lithium hexamethyldisilazane / isopropyl alcohol
3: hydrogenchloride / 1,4-dioxane; dichloromethane
With nickel(II) iodide; hydrogenchloride; carbon tetrabromide; triphenylphosphine; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; dichloromethane; isopropyl alcohol; 2: Suzuki coupling;
DOI:10.1016/j.bmcl.2011.08.048
Guidance literature:
Multi-step reaction with 2 steps
1: nickel(II) iodide; lithium hexamethyldisilazane / isopropyl alcohol
2: hydrogenchloride / 1,4-dioxane; dichloromethane
With nickel(II) iodide; hydrogenchloride; lithium hexamethyldisilazane; In 1,4-dioxane; dichloromethane; isopropyl alcohol; 1: Suzuki coupling;
DOI:10.1016/j.bmcl.2011.08.048
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