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chloro-4-pentadecylphenylmethyl phosphonic acid

Base Information
  • Chemical Name:chloro-4-pentadecylphenylmethyl phosphonic acid
  • CAS No.:1306685-16-4
  • Molecular Formula:C22H38ClO3P
  • Molecular Weight:416.969
  • Hs Code.:
chloro-4-pentadecylphenylmethyl phosphonic acid

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Chemical Property of chloro-4-pentadecylphenylmethyl phosphonic acid
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Technology Process of chloro-4-pentadecylphenylmethyl phosphonic acid

There total 8 articles about chloro-4-pentadecylphenylmethyl phosphonic acid 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:
chloro-4-pentadecylphenylmethyl phosphonic acid dimethyl ester; With trimethylsilyl bromide; In acetonitrile; for 1h; Reflux; Inert atmosphere;
With methanol; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1002/cmdc.201000425
Guidance literature:
Multi-step reaction with 6 steps
1.1: 20 % Pd(OH)2/C; hydrogen / methanol / 2 h / 20 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere
3.1: dipyridinium dichromate / dichloromethane / 16 h / 20 °C / Inert atmosphere
4.1: triethylamine / 4 h / 0 - 20 °C / Inert atmosphere
5.1: thionyl chloride / dichloromethane / 1 h / Reflux; Inert atmosphere
6.1: trimethylsilyl bromide / acetonitrile / 1 h / Reflux; Inert atmosphere
6.2: 0.5 h / 20 °C / Inert atmosphere
With lithium aluminium tetrahydride; dipyridinium dichromate; thionyl chloride; trimethylsilyl bromide; 20 % Pd(OH)2/C; hydrogen; triethylamine; In tetrahydrofuran; methanol; dichloromethane; acetonitrile; 4.1: Pudovic reaction;
DOI:10.1002/cmdc.201000425
Guidance literature:
Multi-step reaction with 7 steps
1.1: palladium diacetate; triethylamine / N,N-dimethyl-formamide / 16 h / Reflux; Inert atmosphere
2.1: 20 % Pd(OH)2/C; hydrogen / methanol / 2 h / 20 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere
4.1: dipyridinium dichromate / dichloromethane / 16 h / 20 °C / Inert atmosphere
5.1: triethylamine / 4 h / 0 - 20 °C / Inert atmosphere
6.1: thionyl chloride / dichloromethane / 1 h / Reflux; Inert atmosphere
7.1: trimethylsilyl bromide / acetonitrile / 1 h / Reflux; Inert atmosphere
7.2: 0.5 h / 20 °C / Inert atmosphere
With lithium aluminium tetrahydride; dipyridinium dichromate; thionyl chloride; trimethylsilyl bromide; 20 % Pd(OH)2/C; hydrogen; palladium diacetate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.1: Heck reaction / 5.1: Pudovic reaction;
DOI:10.1002/cmdc.201000425
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