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4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride

Base Information
  • Chemical Name:4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride
  • CAS No.:93408-26-5
  • Molecular Formula:C17H18Cl2O2
  • Molecular Weight:325.235
  • Hs Code.:
4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride

Synonyms:4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride

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Chemical Property of 4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride
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Technology Process of 4,4-[1,3-propanediylbis(oxy)]bisbenzyl chloride

There total 4 articles about 4,4-[1,3-propanediylbis(oxy)]bisbenzyl 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 thionyl chloride; In dichloromethane; at 0 ℃; for 5h; Inert atmosphere; Reflux;
DOI:10.1021/acsmedchemlett.8b00389
Guidance literature:
Multi-step reaction with 3 steps
1.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 0 - 90 °C
1.2: 1 h / 90 °C
2.1: sodium tetrahydroborate / methanol; tetrahydrofuran / 6 h / 0 - 20 °C
3.1: thionyl chloride / dichloromethane / 5 h / 0 °C / Inert atmosphere; Reflux
With sodium tetrahydroborate; thionyl chloride; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acsmedchemlett.8b00389
Guidance literature:
Multi-step reaction with 2 steps
1: sodium tetrahydroborate / methanol; tetrahydrofuran / 6 h / 0 - 20 °C
2: thionyl chloride / dichloromethane / 5 h / 0 °C / Inert atmosphere; Reflux
With sodium tetrahydroborate; thionyl chloride; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/acsmedchemlett.8b00389
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