2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:181705-84-0
Molecular Formula:C₃₀H₄₁NO₅Si
Molecular Weight:523.745
Hs Code.:

2-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid <i>tert</i>-butyl ester

Synonyms:2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of 2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Supply Marketing:

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 1 raw suppliers

Chemical Property of 2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 10 articles about 2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic 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: 96.0%

: 181705-70-4
(5S,2'S,5'S)-5-[1'-(tert-butoxycarbonyl)-5'-(tert-butyldiphenylsilyloxymethyl)pyrrolidin-2'-yl]-2(5H)-furanone

: 181705-84-0
2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1016/S0960-894X(99)00669-1

Reference yield:

: 138629-30-8,138871-56-4
(S)-tert-butyl 2-((tert-butyldiphenylsilyloxy)methyl)-5-oxopyrrolidine-1-carboxylate

: 181705-84-0
2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: LiEt₃BH / tetrahydrofuran / 3 h / -78 °C

2: BF₃*OEt₂ / diethyl ether / 0.5 h / 20 °C

3: 78 percent / TBSOTf / CH₂Cl₂ / 1 h / -80 °C

4: 90 percent / H₂; AcONa / Pd/C / tetrahydrofuran / 24 h / 20 °C

With boron trifluoride diethyl etherate; t-butyldimethylsiyl triflate; hydrogen; sodium acetate; lithium triethylborohydride; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; 1: Reduction / 2: Alkylation / 3: Mannich reaction / 4: Catalytic hydrogenation;
DOI:10.1002/(SICI)1099-0690(199906)1999:6<1395::AID-EJOC1395>3.0.CO;2-T

Reference yield:

: 81658-25-5,344884-10-2
2-hydroxymethyl-5-oxopyrrolidine-1-carboxylic acid tert-butyl ester

: 181705-84-0
2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-oxo-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 83 percent / imidazole / dimethylformamide / 18 h / 20 °C

2: LiEt₃BH / tetrahydrofuran / 3 h / -78 °C

3: BF₃*OEt₂ / diethyl ether / 0.5 h / 20 °C

4: 78 percent / TBSOTf / CH₂Cl₂ / 1 h / -80 °C

5: 90 percent / H₂; AcONa / Pd/C / tetrahydrofuran / 24 h / 20 °C

With 1H-imidazole; boron trifluoride diethyl etherate; t-butyldimethylsiyl triflate; hydrogen; sodium acetate; lithium triethylborohydride; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; 1: Substitution / 2: Reduction / 3: Alkylation / 4: Mannich reaction / 5: Catalytic hydrogenation;
DOI:10.1002/(SICI)1099-0690(199906)1999:6<1395::AID-EJOC1395>3.0.CO;2-T