(E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

Base Information

Chemical Name:(E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine
CAS No.:1380424-55-4
Molecular Formula:C₂₄H₂₇NO₅
Molecular Weight:409.482
Hs Code.:

Synonyms:(E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

Suppliers and Price of (E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

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Technology Process of (E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

There total 2 articles about (E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine 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: 89.0%

: 99-90-1
para-bromoacetophenone

: 121561-52-2
benzyl tert-butyl N-allyliminodicarbonate

: 1380424-55-4
(E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

Guidance literature:: With palladium diacetate; potassium carbonate; hydroquinone; In N,N-dimethyl-formamide; at 85 ℃; for 12h; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2012.02.081

Reference yield: 75.0%

: 121561-52-2
benzyl tert-butyl N-allyliminodicarbonate

: 149104-90-5
4-acetylphenylboronic acid

: 1380424-55-4
(E)-N-carbobenzyloxy-N-tert-butoxycarbonyl-3-(4-acetylphenyl)prop-2-en-1-amine

Guidance literature:: With potassium hydrogen difluoride; silver(I) acetate; palladium diacetate; In acetone; at 60 ℃; for 8h; stereoselective reaction; Sealed tube;
DOI:10.1002/adsc.201300225