1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

Base Information

Chemical Name:1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone
CAS No.:1027202-80-7
Molecular Formula:C₂₁H₃₅NO₃SSi
Molecular Weight:409.665
Hs Code.:

Synonyms:1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

Suppliers and Price of 1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

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 1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

There total 1 articles about 1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone 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:

: 103-04-8
(phenylthio)acetic acid

: 1027202-80-7
1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: imidazole / dimethylformamide / 12 h / 20 °C

With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1021/jo0259717

Reference yield:

: 1027202-80-7
1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

: 466689-95-2
2-benzenesulfonyl-2-diazo-1-(2,2,5-trimethyl-4-(t-butyldimethyl-silanyloxymethyl)-oxazolidin-3-yl)-ethanone

Guidance literature:: 1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone; With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 1h;

With 4-acetamidobenzenesulfonyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 0 ℃; for 1h; Further stages.;
DOI:10.1021/jo0259717

Reference yield:

: 1027202-80-7
1-[(4R,5R)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2,5-trimethyl-oxazolidin-3-yl]-2-phenylsulfanyl-ethanone

: 6-benzenesulfonyl-1,3,3-trimethyl-7-(t-butyldimethyl-silanyloxymethyl)-tetrahydro-pyrrolo[1,2-c]oxazol-5-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: m-CPBA / CH₂Cl₂ / 1 h / 20 °C

1.2: p-ABSA; DBU / acetonitrile / 1 h / 0 °C

2.1: 94 percent / Rh₂(OAc)4 / CH₂Cl₂ / Heating

With dirhodium tetraacetate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jo0259717