tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

Base Information

Chemical Name:tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate
CAS No.:1352347-55-7
Molecular Formula:C₂₃H₃₉NO₃Si
Molecular Weight:405.653
Hs Code.:

Synonyms:tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

Suppliers and Price of tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

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 tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

There total 1 articles about tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate 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:

: 1352347-54-6
(R)-tert-butyl 3-oxo-1-phenylhex-5-en-2-ylcarbamate

: 1352347-55-7
tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium tri-t-butoxyaluminum hydride / ethanol / 2 h / -78 °C / Inert atmosphere

2: 1H-imidazole; dmap / N,N-dimethyl-formamide / 0 - 20 °C

With 1H-imidazole; dmap; lithium tri-t-butoxyaluminum hydride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2011.07.049

Reference yield: 68.0%

: 1352347-55-7
tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

: 1337862-75-5
(2R,3S)-tert-butyl 2-benzyl-3-(tert-butyldimethylsilyloxy)-5-oxopyrrolidine-1-carboxylate

Guidance literature:: With sodium periodate; ruthenium(III) trichloride hydrate; In tetrachloromethane; water; acetonitrile; at 20 ℃; for 16h;
DOI:10.1016/j.tet.2011.07.049

Reference yield:

: 1352347-55-7
tert-butyl (2R,3S)-3-(tert-butyldimethylsilyloxy)-1-phenylhex-5-en-2-ylcarbamate

: (4R,5R)-5-benzyl-4-hydroxy-2-oxopyrrolidine

Guidance literature:: Multi-step reaction with 5 steps

1: sodium periodate; ruthenium(III) trichloride hydrate / tetrachloromethane; water; acetonitrile / 16 h / 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 20 °C

3: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -78 °C

4: sodium tetrahydroborate / methanol / 2 h / 0 - 20 °C

5: methanol; thionyl chloride / 2 h / 0 - 20 °C

With methanol; sodium tetrahydroborate; sodium periodate; thionyl chloride; oxalyl dichloride; ruthenium(III) trichloride hydrate; tetrabutyl ammonium fluoride; dimethyl sulfoxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.tet.2011.07.049