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2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride

Base Information Edit
  • Chemical Name:2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride
  • CAS No.:162360-26-1
  • Molecular Formula:C16H27NO3*ClH
  • Molecular Weight:317.856
  • Hs Code.:
  • Mol file:162360-26-1.mol
2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride

Synonyms:2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride

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Chemical Property of 2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride Edit
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Technology Process of 2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride

There total 11 articles about 2-amino-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diol hydrochloride 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:
2-acetamido-2-(4-(pentanetyloxy)phenethyl)propane-1,3-diyl diacetate; With lithium hydroxide; In methanol; water; Reflux;
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 3h;
DOI:10.1039/c8cc05643a
Guidance literature:
Multi-step reaction with 4 steps
1.1: triethylamine; dmap / tetrahydrofuran / 72 h / 20 °C
2.1: palladium on activated carbon; hydrogen / ethanol / 0.75 h / 20 °C
3.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C / Schlenk technique; Inert atmosphere
4.1: lithium hydroxide / water; methanol / Reflux
4.2: 3 h / 20 °C
With dmap; palladium on activated carbon; hydrogen; caesium carbonate; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1039/c8cc05643a
Guidance literature:
Multi-step reaction with 9 steps
1.1: methyl-triphenylphosphonium iodide; sodium hydride / tetrahydrofuran / 20 °C
2.1: borane-THF / 0 - 20 °C
2.2: 0 - 20 °C
3.1: iodine; triphenylphosphine; 1H-imidazole / dichloromethane / 0 - 20 °C
4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.75 h / 20 °C / Schlenk technique
4.2: 40 h / 95 °C / Schlenk technique
5.1: lithium chloride; sodium tetrahydroborate / tetrahydrofuran / 60 h / 0 - 20 °C
6.1: triethylamine; dmap / tetrahydrofuran / 72 h / 20 °C
7.1: palladium on activated carbon; hydrogen / ethanol / 0.75 h / 20 °C
8.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C / Schlenk technique; Inert atmosphere
9.1: lithium hydroxide / water; methanol / Reflux
9.2: 3 h / 20 °C
With 1H-imidazole; dmap; sodium tetrahydroborate; borane-THF; palladium on activated carbon; hydrogen; iodine; methyl-triphenylphosphonium iodide; sodium hydride; caesium carbonate; triethylamine; triphenylphosphine; lithium chloride; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1039/c8cc05643a
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