Propanoic acid, 3-(diphenylphosphino)-, ethyl ester

Base Information

• Chemical Name: Propanoic acid, 3-(diphenylphosphino)-, ethyl ester
• CAS No.: 94995-57-0
• Molecular Formula: C17H19O2P
• Molecular Weight: 286.31
• NSC Number: 132582
• DSSTox Substance ID: DTXSID90299769
• Nikkaji Number: J1.958.956K
• Wikidata: Q82042416

Synonyms:Propanoic acid, 3-(diphenylphosphino)-, ethyl ester;94995-57-0;NSC132582;SCHEMBL10837900;DTXSID90299769;GZCCYBGMJFTJRR-UHFFFAOYSA-N;ethyl-3-diphenylphosphinopropionate;NSC-132582

Chemical Property of Propanoic acid, 3-(diphenylphosphino)-, ethyl ester

Chemical Property:

• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 286.11226684
• Heavy Atom Count: 20
• Complexity: 263

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)CCP(C1=CC=CC=C1)C2=CC=CC=C2

Technology Process of Propanoic acid, 3-(diphenylphosphino)-, ethyl ester

There total 6 articles about Propanoic acid, 3-(diphenylphosphino)-, ethyl ester 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: 96.6%

diphenylphosphane (829-85-6) + ethyl acrylate (140-88-5,9003-32-1) → (2-ethoxycarbonylethyl)diphenylphosphine (94995-57-0)

Guidance literature:

In acetonitrile; at -20 - 25 ℃; Inert atmosphere;

Reference yield: 82.0%

ethyl acrylate (140-88-5,9003-32-1) + (tert-butyldimethylsilyl)diphenylphosphine (678187-53-6) → (2-ethoxycarbonylethyl)diphenylphosphine (94995-57-0)

Guidance literature:

With tetrabutyl ammonium fluoride; water; In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

DOI:10.1016/j.tetlet.2004.10.098

Reference yield: 73.0%

benzaldehyde (100-52-7) + lithium diphenylphosphide (65567-06-8,4541-02-0) + ethyl acrylate (140-88-5,9003-32-1) → Ph2PCH(OH)Ph (53772-42-2) + (2-ethoxycarbonylethyl)diphenylphosphine (94995-57-0)

Guidance literature:

With cesium fluoride; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1016/j.tetlet.2005.05.128

upstream raw materials:

ethyl acrylate

(tert-butyldimethylsilyl)diphenylphosphine

benzaldehyde

diphenylphosphane

Downstream raw materials:

{Ru3(CO)9(μ3-η2-C2tBu)}2(μ4-Hg){Ru3(CO)8(μ3-.eta2-C2tBu)(PPh3(CH2CH2COOC2H5))}

{Ru3(CO)9(μ3-η2-C2tBu)(PPh3(CH2CH2COOC2H5))}2(μ4-Hg)

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