Benzeneacetonitrile, a-(2-propenylamino)-

Base Information

Chemical Name:Benzeneacetonitrile, a-(2-propenylamino)-
CAS No.:86926-55-8
Molecular Formula:C11H12N2
Molecular Weight:172.23
Hs Code.:

Synonyms:

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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 Benzeneacetonitrile, a-(2-propenylamino)-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Benzeneacetonitrile, a-(2-propenylamino)-

There total 8 articles about Benzeneacetonitrile, a-(2-propenylamino)- 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: 97.0%

: 7677-24-9
trimethylsilyl cyanide

: 68003-55-4
(E)-N-allylbenzylideneimine

: 86926-55-8
phenyl(prop-2-en-1-ylamino)acetonitrile

Guidance literature:: With lithium perchlorate; In acetonitrile; at 20 ℃; for 10h;
DOI:10.1016/j.tetlet.2004.11.015

Reference yield: 96.0%

: potassium cyanide

: 100-52-7
benzaldehyde

: 107-11-9,30551-89-4
1-amino-2-propene

: 86926-55-8
phenyl(prop-2-en-1-ylamino)acetonitrile

Guidance literature:: benzaldehyde; 1-amino-2-propene; In methanol; at 20 ℃; for 2.5h;

potassium cyanide; With acetic acid; In methanol; at 20 ℃; for 3h;
DOI:10.1515/znb-2016-0005

Reference yield: 87.0%

: 7677-24-9
trimethylsilyl cyanide

: 10283-95-1
N-allylbenzamide

: 86926-55-8
phenyl(prop-2-en-1-ylamino)acetonitrile

Guidance literature:: N-allylbenzamide; With chlorobis(cyclooctene)-iridium(I) dimer; H₂SiEt₂; In toluene; at 20 ℃; for 0.25h; Glovebox; Inert atmosphere;

trimethylsilyl cyanide; With yttrium(III) trifluoromethanesulfonate; In toluene; at 20 ℃; for 1h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.8b02421