2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

Base Information

Chemical Name:2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane
CAS No.:137871-64-8
Molecular Formula:C₃₀H₅₀O₆S₃Si₂
Molecular Weight:659.092
Hs Code.:

2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

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Chemical Property of 2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

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Technology Process of 2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

There total 4 articles about 2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane 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: 78.0%

: 69739-34-0
t-butyldimethylsiyl triflate

: 137871-70-6,137871-76-2
Carbonic acid 1-[2-((E)-5-benzenesulfonyl-3-hydroxy-pent-4-enyl)-[1,3]dithian-2-yl]-2-trimethylsilanylmethyl-allyl ester methyl ester

: 137871-64-8,137871-77-3
2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

Guidance literature:: With dmap; In acetonitrile; 0 deg C to room temperature, 2 h;
DOI:10.1021/jo00028a052

Reference yield:

: 133445-41-7
<(p-chlorophenyl)sulfinyl>(phenylsulfonyl)methane

: 137871-64-8,137871-77-3
2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / piperidine / acetonitrile / 1.5 h / Ambient temperature

2: 78 percent / DMAP / acetonitrile / 0 deg C to room temperature, 2 h

With piperidine; dmap; In acetonitrile;
DOI:10.1021/jo00028a052

Reference yield:

: 137871-60-4
2-(4-hydroxybutyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

: 137871-64-8,137871-77-3
2-((E)-5-(phenylsulfonyl)-3-((tert-butyldimethylsilyl)oxy)-4-pentenyl)-2-(1-((methoxycarbonyl)oxy)-2-((trimethylsilyl)methyl)-2-propenyl)-1,3-dithiane

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / PCC, Celite / CH₂Cl₂ / 2 h / Ambient temperature

2: 86 percent / piperidine / acetonitrile / 1.5 h / Ambient temperature

3: 78 percent / DMAP / acetonitrile / 0 deg C to room temperature, 2 h

With piperidine; dmap; Celite; pyridinium chlorochromate; In dichloromethane; acetonitrile;
DOI:10.1021/jo00028a052