diethyl m-phenoxybenzylidenemalonate

Base Information

Chemical Name:diethyl m-phenoxybenzylidenemalonate
CAS No.:866153-65-3
Molecular Formula:C₂₀H₂₀O₅
Molecular Weight:340.376
Hs Code.:

Synonyms:diethyl m-phenoxybenzylidenemalonate

Suppliers and Price of diethyl m-phenoxybenzylidenemalonate

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 diethyl m-phenoxybenzylidenemalonate

Chemical Property:

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Technology Process of diethyl m-phenoxybenzylidenemalonate

There total 1 articles about diethyl m-phenoxybenzylidenemalonate 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:

: 39515-51-0
3-Phenoxybenzaldehyde

: 105-53-3
diethyl malonate

: 866153-65-3
diethyl m-phenoxybenzylidenemalonate

Guidance literature:: With piperidine; In ethanol; for 3.5h; Heating;
DOI:10.1016/j.bmc.2006.10.010

Reference yield: 93.0%

: 866153-65-3
diethyl m-phenoxybenzylidenemalonate

: 17822-51-4
1-benzylidene-3-oxo-1-pyrazolidinium-2-ide

: (1R,3R)-diethyl 5-oxo-3-(3-phenoxyphenyl)-1-phenyltetrahydropyrazolo[1,2-a]pyrazole-2,2(1H)-dicarboxylate

Guidance literature:: With C₂₃H₄₄N₄O₄; nickel(II) perchlorate hexahydrate; In dichloromethane; at 30 ℃; for 20h; enantioselective reaction; Inert atmosphere; Sealed tube;
DOI:10.1002/chem.201203891

Reference yield: 90.0%

: 866153-65-3
diethyl m-phenoxybenzylidenemalonate

: 120-72-9
indole

: ethyl 2-ethoxycarbonyl-3-(3-indolyl)-3-(m-phenoxylphenyl)propanoate

Guidance literature:: With CF₃O₃S^(1-)*C₃₇H₅₁F₃N₄O₈SSc⁽¹⁺⁾; In diethyl ether; at -20 ℃; for 84h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2009.12.032