triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

Base Information

Chemical Name:triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane
CAS No.:489441-97-6
Molecular Formula:C₂₄H₄₂O₃SSi
Molecular Weight:438.747
Hs Code.:

Synonyms:triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

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Chemical Property of triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

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Technology Process of triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

There total 5 articles about triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane 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:

: 56069-39-7
diethyl phenylsulfonylmethylphosphonate

: 489441-97-6
triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

Guidance literature:: Multi-step reaction with 3 steps

1: 6.0 g / lithium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / -10 - 20 °C

2: diisobutylaluminum hydride / toluene; tetrahydrofuran / 2 h

3: 1.77 g / N,N'-diisopropylethylamine / CH₂Cl₂ / 0.5 h / 20 °C

With diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane; toluene; acetonitrile; 1: Wittig reaction;
DOI:10.1021/ol0271436

Reference yield:

: 80522-42-5
triisopropylsilyl trifluoromethanesulfonate

: (E)-6-Benzenesulfonyl-4-isopropyl-hex-5-en-1-ol

: 489441-97-6
triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1021/ol0271436

Reference yield:

: 70687-49-9
methyl 4-isopropyl-5-oxopentanoate

: 489441-97-6
triisopropyl {[(5E)-4-isopropyl-6-(phenylsulfonyl)hex-5-enyl]oxy}silane

Guidance literature:: Multi-step reaction with 3 steps

1: 6.0 g / lithium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / -10 - 20 °C

2: diisobutylaluminum hydride / toluene; tetrahydrofuran / 2 h

3: 1.77 g / N,N'-diisopropylethylamine / CH₂Cl₂ / 0.5 h / 20 °C

With diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane; toluene; acetonitrile; 1: Wittig reaction;
DOI:10.1021/ol0271436