[(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane

Base Information

• Chemical Name: [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane
• CAS No.: 358753-68-1
• Molecular Formula: C₂₃H₃₄O₅Si
• Molecular Weight: 418.605
• Mol file: 358753-68-1.mol

Synonyms:[(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane

Chemical Property of [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane

There total 4 articles about [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-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%

chloro-trimethyl-silane (75-77-4) + vinylmagnesium chloride (3536-96-7) + (1R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-bicyclo[3.2.1]oct-3-en-2-one (358753-67-0) → [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane (358753-68-1)

Guidance literature:

With copper(I) bromide dimethylsulfide complex; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide;

DOI:10.1039/b101668g

Reference yield:

1,2-dimethoxybenzene (91-16-7) → [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane (358753-68-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: BuLi / -78 °C

1.2: tetrahydrofuran / -78 °C

2.1: PCC / CH₂Cl₂

3.1: 75 percent / CuBr*Me₂S / hexamethylphosphoric acid triamide; tetrahydrofuran

With n-butyllithium; copper(I) bromide dimethylsulfide complex; pyridinium chlorochromate; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;

DOI:10.1039/b101668g

Reference yield:

(1S,5S,6S)-6-Methoxymethoxy-bicyclo[3.2.1]oct-3-en-2-one (351033-77-7) → [(1R,4R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]oct-2-en-2-yloxy]-trimethyl-silane (358753-68-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: BuLi / -78 °C

1.2: tetrahydrofuran / -78 °C

2.1: PCC / CH₂Cl₂

3.1: 75 percent / CuBr*Me₂S / hexamethylphosphoric acid triamide; tetrahydrofuran

With n-butyllithium; copper(I) bromide dimethylsulfide complex; pyridinium chlorochromate; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;

DOI:10.1039/b101668g

upstream raw materials:

chloro-trimethyl-silane

vinylmagnesium chloride

(1R,5S,7S)-4-(2,3-Dimethoxy-phenyl)-7-methoxymethoxy-bicyclo[3.2.1]oct-3-en-2-one

1,2-dimethoxybenzene

Downstream raw materials:

1,2,3,3a(R),9a(R),9b(S)-hexahydro-5-methoxy-9b-[2-[N-methyl-N-(phenylsulfonyl)amino]ethyl]-3-(ethylenedioxy)phenanthro[4,4a,4b,5-bcd]furan

(1R,4S,5S,7S)-3-Bromo-4-(2,3-dimethoxy-phenyl)-7-methoxymethoxy-4-vinyl-bicyclo[3.2.1]octan-2-one