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(E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid

Base Information
  • Chemical Name:(E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid
  • CAS No.:1307803-26-4
  • Molecular Formula:C17H26O3Si
  • Molecular Weight:306.477
  • Hs Code.:
(E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid

Synonyms:(E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid

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Chemical Property of (E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid
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Technology Process of (E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic acid

There total 5 articles about (E)-3-[(tert-butyldimethylsilyl)oxy]-5-phenylpent-4-enoic 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:
3-(tert-butyldimethylsilyloxy)-5-phenylpent-4-enoic acid ethyl ester; With sodium hydroxide; In tetrahydrofuran; methanol; water; at 20 ℃; for 3h;
With hydrogenchloride; In tetrahydrofuran; methanol; water;
DOI:10.1021/np200033y
Guidance literature:
With cesium hydroxide; In 1,4-dioxane; water; at 20 ℃; for 0.833333h;
DOI:10.1039/c7cc04033d
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium diisopropyl amide / tetrahydrofuran / 0.75 h / -78 °C / Inert atmosphere
1.2: Inert atmosphere
2.1: 1H-imidazole / tetrahydrofuran / 12 h / Reflux
3.1: sodium hydroxide / tetrahydrofuran; methanol; water / 3 h / 20 °C
With 1H-imidazole; sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; methanol; water;
DOI:10.1021/np200033y
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