3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

Base Information

Chemical Name:3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan
CAS No.:870776-90-2
Molecular Formula:C₂₆H₂₄O₅S
Molecular Weight:448.54
Hs Code.:

Synonyms:3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

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Chemical Property of 3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

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Technology Process of 3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

There total 9 articles about 3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan 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: 98.0%

: 870776-89-9
2-(3-hydroxyprop-1-ynyl)-3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]furan

: 4972-29-6
benzenesulphinyl chloride

: 870776-90-2
3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at -78 ℃; for 1.5h;
DOI:10.1016/j.tet.2005.08.088

Reference yield:

: 2-iodo-furan-3-carbaldehyde

: 870776-90-2
3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

Guidance literature:: Multi-step reaction with 8 steps

1: TsOH / H₂O; benzene / 1.5 h / Heating

2: 4.49 g / triethylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 20 °C

3: aq. HCl / tetrahydrofuran / 1 h / 20 °C

4: diethyl ether / 1 h / 20 °C

5: 95 percent / ethyldiisopropylamine / CH₂Cl₂ / 9 h / 20 °C

6: 90 percent / tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

7: 91 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 20 °C

8: 98 percent / ethyldiisopropylamine / tetrahydrofuran / 1.5 h / -78 °C

With hydrogenchloride; copper(l) iodide; tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; triethylamine; diisopropylamine; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; diethyl ether; dichloromethane; water; benzene;
DOI:10.1016/j.tet.2005.08.088

Reference yield:

: 2-iodo-3-(1,3-dioxolan-2-yl)furan

: 870776-90-2
3-[1-(methoxymethoxy)-5-phenylpent-4-ynyl]-2-[3-(phenylsulfinyloxy)prop-1-ynyl]furan

Guidance literature:: Multi-step reaction with 7 steps

1: 4.49 g / triethylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 20 °C

2: aq. HCl / tetrahydrofuran / 1 h / 20 °C

3: diethyl ether / 1 h / 20 °C

4: 95 percent / ethyldiisopropylamine / CH₂Cl₂ / 9 h / 20 °C

5: 90 percent / tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

6: 91 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 20 °C

7: 98 percent / ethyldiisopropylamine / tetrahydrofuran / 1.5 h / -78 °C

With hydrogenchloride; copper(l) iodide; tetrabutyl ammonium fluoride; triethylamine; diisopropylamine; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/j.tet.2005.08.088