(E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

Base Information

Chemical Name:(E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline
CAS No.:1170699-62-3
Molecular Formula:C₂₁H₂₉NO₂Si
Molecular Weight:355.552
Hs Code.:

Synonyms:(E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

Suppliers and Price of (E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

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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-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

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Technology Process of (E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

There total 1 articles about (E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline 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: 87.0%

: 104-94-9
4-methoxy-aniline

: 124414-07-9
1-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethanone

: 1170699-62-3
(E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

Guidance literature:: With toluene-4-sulfonic acid; In benzene; for 10h; Reflux;
DOI:10.1021/jo900561h

Reference yield: 72.0%

: 1170699-62-3
(E)-N-{1-[3-(tert-butyldimethylsilyloxy)phenyl]ethylidene}-4-methoxyaniline

: 1170700-12-5
(-)-N-(1-[3-(tert-butyldimethylsilyloxy)phenyl]ethyl)-N-(4-methoxyphenyl)amine

Guidance literature:: With (S)-(-)-N-(3',5'-di-tert-butylphenyl)-2-[formyl(methyl)amino]-3-methylbutanamide; trichlorosilane; In toluene; at 18 ℃; for 16h; optical yield given as %ee; enantiospecific reaction; Inert atmosphere;
DOI:10.1021/jo900561h