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1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride

Base Information
  • Chemical Name:1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride
  • CAS No.:1370256-38-4
  • Molecular Formula:C18H18FN*ClH
  • Molecular Weight:303.807
  • Hs Code.:
1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride

Synonyms:1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride

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Chemical Property of 1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride
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Technology Process of 1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride

There total 3 articles about 1-benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridinium chloride 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:
With hydrogenchloride; In 1,2-dimethoxyethane; water; for 7h; Reflux;
DOI:10.1016/j.bmcl.2012.01.122
Guidance literature:
Multi-step reaction with 2 steps
1.1: iodine; magnesium / tetrahydrofuran / Inert atmosphere; Reflux
1.2: 3 h / 20 °C / Inert atmosphere; Cooling with ice
2.1: hydrogenchloride / 1,2-dimethoxyethane; water / 7 h / Reflux
With hydrogenchloride; iodine; magnesium; In tetrahydrofuran; 1,2-dimethoxyethane; water; 1.1: Grignard reaction / 1.2: Grignard reaction;
DOI:10.1016/j.bmcl.2012.01.122
Guidance literature:
Multi-step reaction with 2 steps
1.1: iodine; magnesium / tetrahydrofuran / Inert atmosphere; Reflux
1.2: 3 h / 20 °C / Inert atmosphere; Cooling with ice
2.1: hydrogenchloride / 1,2-dimethoxyethane; water / 7 h / Reflux
With hydrogenchloride; iodine; magnesium; In tetrahydrofuran; 1,2-dimethoxyethane; water; 1.1: Grignard reaction / 1.2: Grignard reaction;
DOI:10.1016/j.bmcl.2012.01.122
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