(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

Base Information

Chemical Name:(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane
CAS No.:361203-45-4
Molecular Formula:C₁₆H₂₁IO₄S₂
Molecular Weight:468.377
Hs Code.:

Synonyms:(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

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Chemical Property of (4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

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Technology Process of (4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

There total 4 articles about (4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane 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: 80.0%

: 361203-42-1
{(4S,5R)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxolan-4-yl}methyl methanesulfonate

: 361203-49-8
(3aR,7aR)-2,2-dimethyl-6-[(p-tolyl)sulfonyl]-3a,7a-dihydro-4H-thiopyrano[3,4-d][1,3]dioxole

: 361203-45-4
(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

Guidance literature:: With sodium iodide; In acetonitrile; for 4h; Heating;
DOI:10.1002/jhet.5570380304

Reference yield:

: 213767-09-0
2,3-O-isopropylidene-L-erythrofuranose

: 361203-45-4
(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

Guidance literature:: Multi-step reaction with 3 steps

1.1: nBuLi / tetrahydrofuran; hexane / -78 - 0 °C

1.2: 61 percent / tetrahydrofuran; hexane / 12 h / -78 - 20 °C

2.1: 80 percent / pyridine / 12 h / 0 - 20 °C

3.1: 80 percent / NaI / acetonitrile / 4 h / Heating

With pyridine; n-butyllithium; sodium iodide; In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1002/jhet.5570380304

Reference yield:

: 59662-65-6
methylthiomethyl p-tolyl sulfone

: 361203-45-4
(4R,5R)-4-(iodomethyl)-2,2-dimethyl-5-[(E)-2-[(p-tolyl)sulfonyl]-2-(methylthio)ethenyl]-1,3-dioxalane

Guidance literature:: Multi-step reaction with 3 steps

1.1: nBuLi / tetrahydrofuran; hexane / -78 - 0 °C

1.2: 61 percent / tetrahydrofuran; hexane / 12 h / -78 - 20 °C

2.1: 80 percent / pyridine / 12 h / 0 - 20 °C

3.1: 80 percent / NaI / acetonitrile / 4 h / Heating

With pyridine; n-butyllithium; sodium iodide; In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1002/jhet.5570380304