6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Base Information

Chemical Name:6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene
CAS No.:124603-56-1
Molecular Formula:C₂₃H₃₇NO₃SSi
Molecular Weight:435.703
Hs Code.:

Synonyms:6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Suppliers and Price of 6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

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Chemical Property of 6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Chemical Property:

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Technology Process of 6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

There total 4 articles about 6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene 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:

: 80522-42-5
triisopropylsilyl trifluoromethanesulfonate

: 124603-56-1
6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / triethylamine / CH₂Cl₂ / 0 °C

2: 51 percent / 1.) selenium / CH₂Cl₂ / 1.) 25 deg C then reflux; 2.) 0 deg C up to 25 deg C

3: 81 percent / selenium dioxide / tetrahydrofuran / 4 h / Heating

With selenium; selenium(IV) oxide; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/0040-4020(95)00696-6

Reference yield:

: 125332-27-6
4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

: 124603-56-1
6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / 1.) selenium / CH₂Cl₂ / 1.) 25 deg C then reflux; 2.) 0 deg C up to 25 deg C

2: 81 percent / selenium dioxide / tetrahydrofuran / 4 h / Heating

With selenium; selenium(IV) oxide; In tetrahydrofuran; dichloromethane;
DOI:10.1016/0040-4020(95)00696-6

Reference yield:

: 127-65-1
chloroamine-T

: 124603-56-1
6-(4-methylphenylsulfonyl)imino-4-methyl-1-triisopropylsilyl(oxy)-cyclohex-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / 1.) selenium / CH₂Cl₂ / 1.) 25 deg C then reflux; 2.) 0 deg C up to 25 deg C

2: 81 percent / selenium dioxide / tetrahydrofuran / 4 h / Heating

With selenium; selenium(IV) oxide; In tetrahydrofuran; dichloromethane;
DOI:10.1016/0040-4020(95)00696-6