4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

Base Information

Chemical Name:4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one
CAS No.:915038-39-0
Molecular Formula:C₂₁H₁₆O₅S
Molecular Weight:380.421
Hs Code.:

4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5<i>H</i>-furan-2-one

Synonyms:4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

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Chemical Property of 4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

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Technology Process of 4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

There total 5 articles about 4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one 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: 55.0%

: 915038-37-8
3-[4-(3-hydroxybut-1-ynyl)phenyl]-4-(4-methanesulfonylphenyl)-2(5H)furanone

: 915038-39-0
4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

Guidance literature:: With jones reagent; at 0 ℃; for 1h;
DOI:10.1016/j.bmc.2006.07.047

Reference yield:

: 1798-06-7
(4-iodophenyl)acetic acid

: 915038-39-0
4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / cuprous iodide; triethylamine / dichlorobis(triphenylphosphine)palladium / 50 °C

2: triethylamine / acetonitrile / 0.5 h / 25 °C

3: triethylamine; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.83 h / 0 °C

4: 55 percent / Jones reagent / 1 h / 0 °C

With copper(l) iodide; jones reagent; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In acetonitrile; 1: Sonogashira coupling;
DOI:10.1016/j.bmc.2006.07.047

Reference yield:

: 1197-55-3
4-aminophenylacetic acid

: 915038-39-0
4-(4-methanesulfonyl-phenyl)-3-[4-(3-oxo-but-1-ynyl)-phenyl]-5H-furan-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium nitrite; sulfuric acid / H₂O / 0.5 h / 0 °C

1.2: 69 percent / KI / H₂O / 2.5 h / 0 °C

2.1: 91 percent / cuprous iodide; triethylamine / dichlorobis(triphenylphosphine)palladium / 50 °C

3.1: triethylamine / acetonitrile / 0.5 h / 25 °C

4.1: triethylamine; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.83 h / 0 °C

5.1: 55 percent / Jones reagent / 1 h / 0 °C

With copper(l) iodide; jones reagent; sulfuric acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; sodium nitrite; bis-triphenylphosphine-palladium(II) chloride; In water; acetonitrile; 2.1: Sonogashira coupling;
DOI:10.1016/j.bmc.2006.07.047