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(E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid

Base Information
  • Chemical Name:(E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid
  • CAS No.:949162-00-9
  • Molecular Formula:C14H16INO4
  • Molecular Weight:389.19
  • Hs Code.:
(E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid

Synonyms:(E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid

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Chemical Property of (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid
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Technology Process of (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid

There total 13 articles about (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic 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:
With lithium hydroxide; In methanol; water; at 20 ℃; for 36h;
DOI:10.1071/CH06324
Guidance literature:
Multi-step reaction with 9 steps
1.1: 100 percent / hydrogen / platinum(IV) oxide / ethyl acetate / 4.5 h
2.1: nitrogen tetroxide / acetonitrile / 1.25 h / -20 °C
3.1: sodium iodide / acetonitrile / -20 - 20 °C
4.1: 92 percent / trifluoroacetic acid / CH2Cl2 / 23 h / 20 °C
5.1: 72 percent / nitric acid / 3.5 h / 0 °C
6.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C
6.2: 82 percent / tetrahydrofuran / 2 h / -78 - 0 °C
7.1: 85 percent / iron; acetic acid / ethanol / 4.5 h / Heating
8.1: 87 percent / sodium hexamethyldisilazide / tetrahydrofuran / -78 - -60 °C
9.1: 98 percent / lithium hydroxide / methanol; H2O / 36 h / 20 °C
With lithium hydroxide; n-butyllithium; hydrogen; nitric acid; sodium hexamethyldisilazane; dinitrogen tetraoxide; iron; acetic acid; trifluoroacetic acid; sodium iodide; platinum(IV) oxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; ethyl acetate; acetonitrile; 6.2: Horner-Wadsworth-Emmons reaction;
DOI:10.1071/CH06324
Guidance literature:
Multi-step reaction with 10 steps
1.1: 94 percent / toluenesulfonic acid / toluene / Heating
2.1: 100 percent / hydrogen / platinum(IV) oxide / ethyl acetate / 4.5 h
3.1: nitrogen tetroxide / acetonitrile / 1.25 h / -20 °C
4.1: sodium iodide / acetonitrile / -20 - 20 °C
5.1: 92 percent / trifluoroacetic acid / CH2Cl2 / 23 h / 20 °C
6.1: 72 percent / nitric acid / 3.5 h / 0 °C
7.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C
7.2: 82 percent / tetrahydrofuran / 2 h / -78 - 0 °C
8.1: 85 percent / iron; acetic acid / ethanol / 4.5 h / Heating
9.1: 87 percent / sodium hexamethyldisilazide / tetrahydrofuran / -78 - -60 °C
10.1: 98 percent / lithium hydroxide / methanol; H2O / 36 h / 20 °C
With lithium hydroxide; n-butyllithium; o-toluenesulfonic acid; hydrogen; nitric acid; sodium hexamethyldisilazane; dinitrogen tetraoxide; iron; acetic acid; trifluoroacetic acid; sodium iodide; platinum(IV) oxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; ethyl acetate; toluene; acetonitrile; 7.2: Horner-Wadsworth-Emmons reaction;
DOI:10.1071/CH06324
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