(E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine

Base Information

Chemical Name:(E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine
CAS No.:1370549-55-5
Molecular Formula:C₂₂H₃₃NO₇
Molecular Weight:423.507
Hs Code.:

Synonyms:(E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)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,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine

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Technology Process of (E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine

There total 2 articles about (E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)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: 91.0%

: 2675-79-8
1-bromo-3,4,5-trimethoxybenzene

: 115269-99-3
N,N-bis(tert-butoxycarbonyl)allylamine

: 1370549-55-5
(E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; palladium diacetate; potassium carbonate; In water; at 90 ℃; for 2h; regioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201100835

Reference yield: 75.0%

: 2675-80-1
1,2,3-trimethoxy-5-chlorobenzene

: 115269-99-3
N,N-bis(tert-butoxycarbonyl)allylamine

: 1370549-55-5
(E)-N,N-bis(tert-butoxycarbonyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-amine

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; palladium diacetate; potassium carbonate; In toluene; at 20 - 125 ℃; for 12h; regioselective reaction; Sealed tube; Inert atmosphere;
DOI:10.1002/cctc.201300755