(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

Base Information

Chemical Name:(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole
CAS No.:170305-70-1
Molecular Formula:C₂₀H₃₁N₃O₂Si
Molecular Weight:373.571
Hs Code.:

Synonyms:(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

Suppliers and Price of (2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

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 0 raw suppliers

Chemical Property of (2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

There total 2 articles about (2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole 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: 91.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 170305-66-5
(2'S)-<1-(5-Phenyl-1,3,4-oxadiazol-2-ylmethyl)pyrrolidin-2'-yl>methanol

: 170305-70-1
(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; Ambient temperature;

Reference yield:

: 33575-83-6
2-(chloromethyl)-5-phenyl-1,3,4-oxadiazole

: 170305-70-1
(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / Et₃N / ethanol / 3 h / Heating

2: 91 percent / imidazole / dimethylformamide / Ambient temperature

With 1H-imidazole; triethylamine; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 106-95-6
allyl bromide

: 170305-70-1
(2'S)-2-(2'-tert-Butyldimethylsilyloxymethylpyrrolidin-1-ylmethyl)-5-phenyl-1,3,4-oxadiazole

: (1'R,2''S)-2-<1'-(2''-tert-Butyldimethylsilyloxymethylpyrrolidin-1-yl)but-3-enyl>-5-phenyl-1,3,4-oxadiazole

: (1'S,2''S)-2-<1'-(2''-tert-Butyldimethylsilyloxymethylpyrrolidin-1-yl)but-3-enyl>-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With triethyl borane; lithium diisopropyl amide; In tetrahydrofuran; hexane; Yield given. Yields of byproduct given. Title compound not separated from byproducts; 1.) -78 deg C, 3 min, 2.) -100 deg C, 1 h; -100 deg C to r.t., overnight;