(2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide

Base Information

• Chemical Name: (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide
• CAS No.: 1279696-96-6
• Molecular Formula: C₁₆H₁₇NO₄S₂
• Molecular Weight: 351.447
• Mol file: 1279696-96-6.mol

Synonyms:(2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide

Chemical Property of (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide

There total 1 articles about (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide 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: 77.0%

(2S)-2-p-toluenesulfonamido-3-phenylpropanol (82495-70-3) → (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide (1279696-96-6)

Guidance literature:

With pyridine; thionyl chloride; In tetrahydrofuran; at -78 ℃; Inert atmosphere;

DOI:10.1002/chem.201003222

Reference yield: 94.0%

(2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide (1279696-96-6) + benzaldehyde (100-52-7) + 2-mesitylmagnesium bromide (2633-66-1) → (2S)-2-p-toluenesulfonamido-3-phenylpropanol (82495-70-3) + (S)-(+)-N-(benzylidene)-2,4,6-trimethylbenzenesulfinamide (855475-24-0)

Guidance literature:

(2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide; 2-mesitylmagnesium bromide; In tetrahydrofuran; at -68 ℃; Inert atmosphere; Cooling with acetone-dry ice;

With lithium hexamethyldisilazane; In tetrahydrofuran; at -68 - 20 ℃; Inert atmosphere;

benzaldehyde; With titanium(IV) tetraethanolate; In tetrahydrofuran; at 20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;

DOI:10.1002/chem.201003222

Reference yield: 85.0%

5-bromo-2-thiophencarboxaldehyde (4701-17-1) + (2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide (1279696-96-6) + 2-mesitylmagnesium bromide (2633-66-1) → (S,E)-N-((5-bromothiophen-2-yl)methylene)-2,4,6-trimethylbenzenesulfinamide (1279697-23-2)

Guidance literature:

(2R,4S)-3-[(4-methylphenyl)sulfonyl]-4-(phenylmethyl)-1,2,3-oxathiazolidine 2-oxide; 2-mesitylmagnesium bromide; In tetrahydrofuran; at -68 ℃; Inert atmosphere; Cooling with acetone-dry ice;

With lithium hexamethyldisilazane; In tetrahydrofuran; at -68 - 20 ℃; Inert atmosphere;

5-bromo-2-thiophencarboxaldehyde; With titanium(IV) tetraethanolate; In tetrahydrofuran; at 20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;

DOI:10.1002/chem.201003222

upstream raw materials:

(2S)-2-p-toluenesulfonamido-3-phenylpropanol

Downstream raw materials:

(S,E)-2,4,6-trimethyl-N-(pyridin-2-ylmethylene)benzenesulfinamide

(S,E)-N-(furan-2-ylmethylene)-2,4,6-trimethylbenzenesulfinamide

(S,E)-2,4,6-trimethyl-N-(thiazol-5-ylmethylene)benzenesulfinamide

(S,E)-N-((E)-3-phenylallylidene)propane-2-sulfinamide