tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane

Base Information

• Chemical Name: tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane
• CAS No.: 191677-96-0
• Molecular Formula: C₃₀H₃₈O₄Si
• Molecular Weight: 490.715
• Mol file: 191677-96-0.mol

Synonyms:tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane

Chemical Property of tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane

There total 5 articles about tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-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: 75.0%

prenyl bromide (870-63-3) + tert-Butyl-(4-methoxy-2-methoxymethoxy-phenoxy)-diphenyl-silane (191677-91-5) → tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane (191677-96-0)

Guidance literature:

With tert.-butyl lithium; In tetrahydrofuran; at 25 ℃;

DOI:10.1016/S0040-4039(97)00927-1

Reference yield:

2-hydroxy-5-methoxybenzaldehyde (672-13-9) → tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane (191677-96-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 90 percent / imidazole / tetrahydrofuran / 25 °C

2: 93 percent / m-CPBA / ethyl acetate / 25 °C

3: 61 percent / NaH / tetrahydrofuran / 25 °C

4: 75 percent / t-BuLi / tetrahydrofuran / 25 °C

With 1H-imidazole; tert.-butyl lithium; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/S0040-4039(97)00927-1

Reference yield:

tert-butylchlorodiphenylsilane (58479-61-1) → tert-Butyl-[4-methoxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenoxy]-diphenyl-silane (191677-96-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 90 percent / imidazole / tetrahydrofuran / 25 °C

2: 93 percent / m-CPBA / ethyl acetate / 25 °C

3: 61 percent / NaH / tetrahydrofuran / 25 °C

4: 75 percent / t-BuLi / tetrahydrofuran / 25 °C

With 1H-imidazole; tert.-butyl lithium; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/S0040-4039(97)00927-1

upstream raw materials:

prenyl bromide

tert-Butyl-(4-methoxy-2-methoxymethoxy-phenoxy)-diphenyl-silane

2-hydroxy-5-methoxybenzaldehyde

tert-butylchlorodiphenylsilane

Downstream raw materials:

2-(2-Benzo[1,3]dioxol-5-yl-[1,3]dioxolan-2-yl)-1-[8-(tert-butyl-diphenyl-silanyloxy)-5-methoxy-2,2-dimethyl-2H-chromen-6-yl]-ethanone

2-(2-Benzo[1,3]dioxol-5-yl-[1,3]dioxolan-2-yl)-1-[8-(tert-butyl-diphenyl-silanyloxy)-5-methoxy-2,2-dimethyl-2H-chromen-6-yl]-ethanol

tert-Butyl-(5-methoxy-2,2-dimethyl-2H-chromen-8-yloxy)-diphenyl-silane

6-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-2-(3-methyl-but-2-enyl)-phenol