Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester

Base Information Edit
  • Chemical Name:4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester
  • CAS No.:339533-80-1
  • Molecular Formula:C24H34O3Si
  • Molecular Weight:398.618
  • Hs Code.:
  • Mol file:339533-80-1.mol
4-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester

Synonyms:4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester

Suppliers and Price of 4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester
Supply Marketing:Edit
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 4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl ester

There total 13 articles about 4-(tert-butyl-diphenyl-silanyloxymethyl)-hexanoic acid methyl 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:
Guidance literature:
With hydrogen; palladium on activated charcoal; trifluoroacetic acid; In ethanol; for 12h; under 760.051 Torr;
DOI:10.1021/jo001767c
Guidance literature:
Multi-step reaction with 8 steps
1.1: n-BuLi / tetrahydrofuran; various solvent(s) / 1 h / -78 °C
1.2: 100 percent / tetrahydrofuran; various solvent(s) / 1 h / -30 °C
2.1: 48 percent / Lipase PS3O / pentane / 24 h / 20 °C
3.1: 90 percent / K2CO3 / methanol / 13 h / 20 °C
4.1: DMSO; oxalyl chloride; Et3N / CH2Cl2 / -78 - 20 °C
5.1: LiN(Me3Si)2 / tetrahydrofuran / 0.33 h / -10 - 20 °C
5.2: 7.63 g / tetrahydrofuran / 0.5 h / 0 °C
6.1: 83 percent / aq. HF / acetonitrile; CH2Cl2 / 2 h / 20 °C
7.1: 85 percent / imidazole / dimethylformamide / 14 h / -5 - 20 °C
8.1: H2 / Pd/C; TFA / ethanol / 12 h / 760.05 Torr
With 1H-imidazole; n-butyllithium; oxalyl dichloride; Lipase PS3O; hydrogen fluoride; hydrogen; potassium carbonate; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; trifluoroacetic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; pentane;
DOI:10.1021/jo001767c
Guidance literature:
Multi-step reaction with 7 steps
1.1: 48 percent / Lipase PS3O / pentane / 24 h / 20 °C
2.1: 90 percent / K2CO3 / methanol / 13 h / 20 °C
3.1: DMSO; oxalyl chloride; Et3N / CH2Cl2 / -78 - 20 °C
4.1: LiN(Me3Si)2 / tetrahydrofuran / 0.33 h / -10 - 20 °C
4.2: 7.63 g / tetrahydrofuran / 0.5 h / 0 °C
5.1: 83 percent / aq. HF / acetonitrile; CH2Cl2 / 2 h / 20 °C
6.1: 85 percent / imidazole / dimethylformamide / 14 h / -5 - 20 °C
7.1: H2 / Pd/C; TFA / ethanol / 12 h / 760.05 Torr
With 1H-imidazole; oxalyl dichloride; Lipase PS3O; hydrogen fluoride; hydrogen; potassium carbonate; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; trifluoroacetic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; pentane;
DOI:10.1021/jo001767c
Post RFQ for Price