Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

Base Information

Chemical Name:Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate
CAS No.:62596-44-5
Molecular Formula:C14H14O4
Molecular Weight:246.263
Hs Code.:
DSSTox Substance ID:DTXSID80490763
Nikkaji Number:J3.052.038F
Wikidata:Q82334746

Synonyms:Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate;62596-44-5;DTXSID80490763

Suppliers and Price of Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

Supply Marketing:

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

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Chemical Property of Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:246.08920892
Heavy Atom Count:18
Complexity:271

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=COC(=C1)C2=CC=C(C=C2)OC

Technology Process of Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

There total 3 articles about Ethyl 5-(4-methoxyphenyl)furan-3-carboxylate 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: 85.0%

: 1371636-77-9
(E)-ethyl 4-(4-methoxyphenyl)-2-(phenoxymethylene)but-3-ynoate

: 62596-44-5
ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

Guidance literature:: With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; In tetrahydrofuran; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1039/c2ob07173h

Reference yield:

: 1371636-99-5
(Z)-ethyl 2-bromo-3-phenoxyacrylate

: 768-60-5
4-methoxyphenylacetylen

: 62596-44-5
ethyl 5-(4-methoxyphenyl)furan-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / 70 °C / Inert atmosphere

2: (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; triethylamine; In tetrahydrofuran; 1: Sonogashira coupling;
DOI:10.1039/c2ob07173h