Benzeneacetic acid, a-ethyl-a-methyl-, (S)-

Base Information

Chemical Name:Benzeneacetic acid, a-ethyl-a-methyl-, (S)-
CAS No.:3968-68-1
Molecular Formula:C11H14O2
Molecular Weight:178.231
Hs Code.:

Synonyms:

Suppliers and Price of Benzeneacetic acid, a-ethyl-a-methyl-, (S)-

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of Benzeneacetic acid, a-ethyl-a-methyl-, (S)-

Chemical Property:

Purity/Quality:: 95% ^*data from raw suppliers

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Technology Process of Benzeneacetic acid, a-ethyl-a-methyl-, (S)-

There total 17 articles about Benzeneacetic acid, a-ethyl-a-methyl-, (S)- 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: 84.0%

: 768392-48-9
(R)-(-)-3-methyl-3-phenyl-1-pentene

: 3968-68-1
(+)-(2S)-2-Methyl-2-phenylbutanoic acid

Guidance literature:: (R)-(-)-3-methyl-3-phenyl-1-pentene; With ruthenium trichloride; sodium periodate; In tetrachloromethane; water; acetonitrile; at 20 ℃; for 3h; Inert atmosphere;

With sulfuric acid; In dichloromethane; water; optical yield given as %ee; Inert atmosphere;
DOI:10.1021/jo900198b

Reference yield: 76.0%

: 492-37-5,2328-24-7
hydratropic acid

: 75-03-6
ethyl iodide

: 3968-68-1
(+)-(2S)-2-Methyl-2-phenylbutanoic acid

Guidance literature:: hydratropic acid; With n-butyllithium; N¹,N³-bis((R)-1-phenyl-2-(piperidin-1-yl)ethyl)propane-1,3-diamine; In tetrahydrofuran; hexane; at 0 - 20 ℃; for 1h; Inert atmosphere;

ethyl iodide; In tetrahydrofuran; hexane; at -78 ℃; for 0.166667h; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jacs.6b11673