tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane

Base Information

• Chemical Name: tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane
• CAS No.: 204325-21-3
• Molecular Formula: C₂₆H₃₅IOSi
• Molecular Weight: 518.553
• Mol file: 204325-21-3.mol

Synonyms:tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane

Chemical Property of tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane

There total 4 articles about tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-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: 64.0%

4-(tert-Butyl-diphenyl-silanyloxy)-1,1-dicyclopropyl-butan-1-ol (204325-28-0) → tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane (204325-21-3)

Guidance literature:

With N-iodo-succinimide; triphenylphosphine; In dichloromethane; at -30 ℃;

DOI:10.1039/a707320h

Reference yield:

tert-butylchlorodiphenylsilane (58479-61-1) → tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane (204325-21-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 97 percent / imidazole

2: 64 percent / NIS, PPh₃ / CH₂Cl₂ / -30 °C

With 1H-imidazole; N-iodo-succinimide; triphenylphosphine; In dichloromethane;

DOI:10.1039/a707320h

Reference yield:

dicyclopropyl ketone (1121-37-5) → tert-Butyl-((Z)-4-cyclopropyl-7-iodo-hept-4-enyloxy)-diphenyl-silane (204325-21-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 1.) MeMgBr, Mg / 1.) THF, -30 deg C; 70 deg C

2: 97 percent / imidazole

3: 64 percent / NIS, PPh₃ / CH₂Cl₂ / -30 °C

With 1H-imidazole; N-iodo-succinimide; methylmagnesium bromide; magnesium; triphenylphosphine; In dichloromethane;

DOI:10.1039/a707320h

upstream raw materials:

4-(tert-Butyl-diphenyl-silanyloxy)-1,1-dicyclopropyl-butan-1-ol

tert-butylchlorodiphenylsilane

dicyclopropyl ketone

1,1-Dicyclopropyl-butane-1,4-diol

Downstream raw materials:

(Z)-9-(tert-Butyl-diphenyl-silanyloxy)-6-cyclopropyl-2-methylene-non-5-enoic acid methyl ester

(2Z,6Z)-6-Cyclopropyl-10-methylene-2-(3-phenylselanylcarbonyl-propyl)-undeca-2,6-dienedioic acid dimethyl ester

(2Z,6Z)-2-[4-(tert-Butyl-diphenyl-silanyloxy)-butyl]-6-cyclopropyl-10-methylene-undeca-2,6-dienedioic acid dimethyl ester