(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

Base Information

Chemical Name:(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine
CAS No.:881309-46-2
Molecular Formula:C₂₀H₂₄BrNO₄S₂
Molecular Weight:486.451
Hs Code.:

Synonyms:(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

Suppliers and Price of (4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

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 (4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

There total 1 articles about (4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine 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: 70.0%

: N-((1S,2S)-3-Benzenesulfinyl-1-bromomethyl-2-hydroxy-propyl)-4-methyl-benzenesulfonamide

: 77-76-9
2,2-dimethoxy-propane

: 881309-46-2
(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

Guidance literature:: camphor-10-sulfonic acid; In acetone; at 70 ℃; for 6h;
DOI:10.1016/j.tetlet.2005.12.123

Reference yield: 90.0%

: 881309-46-2
(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

: 881309-47-3
(4R,5S)-4-Azidomethyl-5-benzenesulfinylmethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

Guidance literature:: With sodium azide; In dimethyl sulfoxide; at 80 ℃; for 6h;
DOI:10.1016/j.tetlet.2005.12.123

Reference yield:

: 881309-46-2
(4S,5S)-5-Benzenesulfinylmethyl-4-bromomethyl-2,2-dimethyl-3-(toluene-4-sulfonyl)-oxazolidine

: N-(4-isopropoxy-azepan-3-yl)-N-isopropyl-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: 90 percent / NaN₃ / dimethylsulfoxide / 6 h / 80 °C

2.1: trifluoroacetic anhydride / CH₂Cl₂ / 0.5 h / 0 °C

2.2: 70 percent / SnCl₄ / 0.08 h / 0 °C

3.1: O₃ / CH₂Cl₂ / 30 h / -78 °C

3.2: 75 percent / Me₂S / 0.5 h / -78 - 0 °C

4.1: 70 percent / NaBH₄; CeCl₃ / methanol / 0.5 h / 0 °C

5.1: 90 percent / H₂ / Pd/C / 6 h / 20 °C

6.1: 88 percent / Et₃N / DMAP / CH₂Cl₂ / 0.5 h / 0 °C

7.1: 70 percent / KOt-Bu / tetrahydrofuran / 1 h / 20 °C

With sodium tetrahydroborate; sodium azide; cerium(III) chloride; potassium tert-butylate; hydrogen; ozone; triethylamine; trifluoroacetic anhydride; dmap; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; 4.1: Luche reduction;
DOI:10.1016/j.tetlet.2005.12.123