1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

Base Information

Chemical Name:1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene
CAS No.:724755-73-1
Molecular Formula:C₂₀H₂₃IO₃S
Molecular Weight:470.371
Hs Code.:

Synonyms:1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

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Chemical Property of 1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

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Technology Process of 1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

There total 4 articles about 1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene 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:

: 85418-23-1
(S)-1-O-benzyl-1,2,4-butanetriol

: 724755-73-1
1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

Guidance literature:: Multi-step reaction with 3 steps

1.1: 84 percent / triethylamine / CH₂Cl₂ / 12 h / 0 °C

2.1: lithium hexamethyldisilazide / tetrahydrofuran / 1 h / -78 - -20 °C

2.2: 7 percent / tetrahydrofuran / -78 - -20 °C

3.1: 84 percent / NaI / acetone / 3 h / Heating

With triethylamine; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1021/ol049676f

Reference yield:

: 100-39-0
benzyl bromide

: 724755-73-1
1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / tetrahydrofuran

2.1: AcOH; H₂O; NaIO₄ / methanol

3.1: 84 percent / triethylamine / CH₂Cl₂ / 12 h / 0 °C

4.1: lithium hexamethyldisilazide / tetrahydrofuran / 1 h / -78 - -20 °C

4.2: 7 percent / tetrahydrofuran / -78 - -20 °C

5.1: 84 percent / NaI / acetone / 3 h / Heating

With sodium periodate; water; sodium hydride; acetic acid; triethylamine; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; acetone;
DOI:10.1021/ol049676f

Reference yield:

: 139884-79-0
(S)-4-Benzyloxymethyl-2-phenyl-[1,3]dioxane

: 724755-73-1
1-[(S)-(E)-2-((S)-1-Benzyloxymethyl-3-iodo-propoxy)-ethenesulfinyl]-4-methyl-benzene

Guidance literature:: Multi-step reaction with 4 steps

1.1: AcOH; H₂O; NaIO₄ / methanol

2.1: 84 percent / triethylamine / CH₂Cl₂ / 12 h / 0 °C

3.1: lithium hexamethyldisilazide / tetrahydrofuran / 1 h / -78 - -20 °C

3.2: 7 percent / tetrahydrofuran / -78 - -20 °C

4.1: 84 percent / NaI / acetone / 3 h / Heating

With sodium periodate; water; acetic acid; triethylamine; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; acetone;
DOI:10.1021/ol049676f