{(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester
• CAS No.: 197707-19-0
• Molecular Formula: C₃₇H₆₁NO₃Si
• Molecular Weight: 595.982
• Mol file: 197707-19-0.mol

Synonyms:{(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester

Chemical Property of {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester

There total 5 articles about {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester 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: 85.0%

Undecyllithium (98499-04-8) + Toluene-4-sulfonic acid (S)-2-tert-butoxycarbonylamino-5-(tert-butyl-diphenyl-silanyloxy)-pentyl ester (197707-18-9) → {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester (197707-19-0)

Guidance literature:

With copper(l) iodide; In diethyl ether; at -35 ℃;

DOI:10.1016/S0040-4039(97)01759-0

Reference yield:

tert-butyl (4S)-4-(3-hydroxypropyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (136923-04-1) → {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester (197707-19-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 100 percent / imidazole / CH₂Cl₂ / Ambient temperature

2: 98 percent / PdCl₂(CH₃CN)2 / acetonitrile / Heating

3: 97 percent / Et₃N, DMAP / CH₂Cl₂ / Ambient temperature

4: 85 percent / CuI / diethyl ether / -35 °C

With 1H-imidazole; dmap; dichloro bis(acetonitrile) palladium(II); copper(l) iodide; triethylamine; In diethyl ether; dichloromethane; acetonitrile;

DOI:10.1016/S0040-4039(97)01759-0

Reference yield:

tert-butylchlorodiphenylsilane (58479-61-1) → {(R)-1-[3-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester (197707-19-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 100 percent / imidazole / CH₂Cl₂ / Ambient temperature

2: 98 percent / PdCl₂(CH₃CN)2 / acetonitrile / Heating

3: 97 percent / Et₃N, DMAP / CH₂Cl₂ / Ambient temperature

4: 85 percent / CuI / diethyl ether / -35 °C

With 1H-imidazole; dmap; dichloro bis(acetonitrile) palladium(II); copper(l) iodide; triethylamine; In diethyl ether; dichloromethane; acetonitrile;

DOI:10.1016/S0040-4039(97)01759-0

upstream raw materials:

Undecyllithium

Toluene-4-sulfonic acid (S)-2-tert-butoxycarbonylamino-5-(tert-butyl-diphenyl-silanyloxy)-pentyl ester

tert-butyl (4S)-4-(3-hydroxypropyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

tert-butylchlorodiphenylsilane

Downstream raw materials:

Allyl-{(R)-1-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-tridecyl}-carbamic acid tert-butyl ester