N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide
CAS No.:925463-62-3
Molecular Formula:C₃₄H₄₅NO₄SSi
Molecular Weight:591.887
Hs Code.:

<i>N</i>-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Synonyms:N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Suppliers and Price of N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

There total 9 articles about N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide 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: 94.0%

: 925463-61-2
N-(2-benzyloxy-4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

: 13154-24-0
triisopropylsilyl chloride

: 925463-62-3
N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/jo062064j

Reference yield:

: 925463-43-0
4-amino-3-benzyloxy-phenol

: 925463-62-3
N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / pyridine / CH₂Cl₂ / 4 h / 20 °C

2: 96 percent / sodium periodate on silica gel / CH₂Cl₂ / 4 h

3: CH₂Cl₂ / 15 h / 20 °C

4: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 0.33 h / 0 °C

5: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C

With pyridine; sodium periodate; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; 3: Diels-Alder reaction;
DOI:10.1021/jo062064j

Reference yield:

: 221615-94-7
3-(benzyloxy)-4-nitrophenol

: 925463-62-3
N-(2-benzyloxy-8-methyl-4-triisopropylsilanyloxy-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: sodium borohydride; nickel(II) chloride hexahydrate / tetrahydrofuran; methanol

2: 84 percent / pyridine / CH₂Cl₂ / 4 h / 20 °C

3: 96 percent / sodium periodate on silica gel / CH₂Cl₂ / 4 h

4: CH₂Cl₂ / 15 h / 20 °C

5: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 0.33 h / 0 °C

6: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C

With pyridine; sodium tetrahydroborate; sodium periodate; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; 4: Diels-Alder reaction;
DOI:10.1021/jo062064j