(4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester

Base Information

• Chemical Name: (4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester
• CAS No.: 249278-59-9
• Molecular Formula: C₂₀H₃₀N₂O₄
• Molecular Weight: 362.469

Synonyms:(4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester

Chemical Property of (4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of (4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester

There total 1 articles about (4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester 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:

Reference yield: 40.0%

iodobenzene (591-50-4) + (E)-2-(tributylstannyl)-1,4-di(tert-butoxycarbonyl)amino-2-butene → (4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester (249278-59-9)

Guidance literature:

With copper(l) iodide; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; triphenyl-arsane; In various solvent(s); at 50 ℃; for 17h;

DOI:10.1016/S0040-4039(99)01165-X

Reference yield: 100.0%

(4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester (249278-59-9) → (Z)-2-Phenyl-but-2-ene-1,4-diamine; compound with GENERIC INORGANIC NEUTRAL COMPONENT

Guidance literature:

With hydrogenchloride; In ethanol;

DOI:10.1016/S0040-4039(99)01165-X

Reference yield:

(4-tert-butoxycarbonylamino-3-phenyl-but-2-enyl)-carbamic acid tert-butyl ester (249278-59-9) → (4-tert-butoxycarbonylamino-3-phenyl-butyl)-carbamic acid tert-butyl ester

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; under 52504.2 Torr;

DOI:10.1016/S0040-4039(99)01165-X

upstream raw materials:

iodobenzene

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