5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Base Information

Chemical Name:5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde
CAS No.:919608-20-1
Molecular Formula:C₂₄H₃₂O₃Si
Molecular Weight:396.602
Hs Code.:

5-[2-(<i>tert</i>-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Synonyms:5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Suppliers and Price of 5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

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 5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

There total 6 articles about 5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde 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:

: 919608-47-2
5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2-methyl-pentane-1,3-diol

: 919608-20-1
5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Guidance literature:: Multi-step reaction with 5 steps

1: 3.59 g / imidazole / CH₂Cl₂ / 1 h / 20 °C

2: 98 percent / TEA / CH₂Cl₂ / 0 - 20 °C

3: 84 percent / CSA; methanol / 2 h / 20 °C

4: 80 percent / sodium hexamethyldisilazide / tetrahydrofuran / 0 - 20 °C

5: 89 percent / SO₃*pyridine; TEA; DMSO / CH₂Cl₂ / 0.5 h / 20 °C

With 1H-imidazole; methanol; pyridine-SO₃ complex; TEA; camphor-10-sulfonic acid; sodium hexamethyldisilazane; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; 4: Williamson ether synthesis;
DOI:10.1016/j.tet.2007.07.005

Reference yield:

: 919608-12-1
1-(tert-butyl-diphenyl-silanyloxy)-5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2-methyl-pentan-3-ol

: 919608-20-1
5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / TEA / CH₂Cl₂ / 0 - 20 °C

2: 84 percent / CSA; methanol / 2 h / 20 °C

3: 80 percent / sodium hexamethyldisilazide / tetrahydrofuran / 0 - 20 °C

4: 89 percent / SO₃*pyridine; TEA; DMSO / CH₂Cl₂ / 0.5 h / 20 °C

With methanol; pyridine-SO₃ complex; TEA; camphor-10-sulfonic acid; sodium hexamethyldisilazane; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; 3: Williamson ether synthesis;
DOI:10.1016/j.tet.2007.07.005

Reference yield:

: 919608-28-9
3-[5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-3-hydroxy-2-methyl-pentanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

: 919608-20-1
5-[2-(tert-butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-carbaldehyde

Guidance literature:: Multi-step reaction with 6 steps

1: lithium borohydride / diethyl ether; tetrahydrofuran / 0 - 20 °C

2: 3.59 g / imidazole / CH₂Cl₂ / 1 h / 20 °C

3: 98 percent / TEA / CH₂Cl₂ / 0 - 20 °C

4: 84 percent / CSA; methanol / 2 h / 20 °C

5: 80 percent / sodium hexamethyldisilazide / tetrahydrofuran / 0 - 20 °C

6: 89 percent / SO₃*pyridine; TEA; DMSO / CH₂Cl₂ / 0.5 h / 20 °C

With 1H-imidazole; methanol; lithium borohydride; pyridine-SO₃ complex; TEA; camphor-10-sulfonic acid; sodium hexamethyldisilazane; dimethyl sulfoxide; In tetrahydrofuran; diethyl ether; dichloromethane; 5: Williamson ether synthesis;
DOI:10.1016/j.tet.2007.07.005