(S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate

Base Information

• Chemical Name: (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate
• CAS No.: 1008128-93-5
• Molecular Formula: C₂₉H₂₇NO₃S
• Molecular Weight: 469.604
• Mol file: 1008128-93-5.mol

Synonyms:(S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate

Chemical Property of (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate

There total 4 articles about (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate 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: 92.0%

p-toluenesulfonyl chloride (98-59-9) + (S)-N-triphenylmethyl-aziridinylmethanol (152706-23-5) → (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate (1008128-93-5)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 20 ℃; for 16h;

DOI:10.1021/jo7023637

Reference yield:

methyl N-trityl-L-serinate (13515-76-9,116457-91-1,4465-44-5) → (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate (1008128-93-5)

Guidance literature:

Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran / 0.53 h / 0 °C / Inert atmosphere

2: tetrahydrofuran / 48 h / 65 °C / Inert atmosphere

3: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / 0 - 20 °C / Inert atmosphere

4: triethylamine; dmap / dichloromethane / 24 h / 0 - 20 °C / Inert atmosphere

With dmap; lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.tetlet.2016.06.101

Reference yield:

(S)-methyl3-((methylsulfonyl)oxy)-2-(tritylamino)propanoate (76357-12-5) → (S)-(1-tritylaziridin-2-yl)methyl 4-methylbenzenesulfonate (1008128-93-5)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / 48 h / 65 °C / Inert atmosphere

2: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / 0 - 20 °C / Inert atmosphere

3: triethylamine; dmap / dichloromethane / 24 h / 0 - 20 °C / Inert atmosphere

With dmap; lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.tetlet.2016.06.101

upstream raw materials:

p-toluenesulfonyl chloride

(S)-N-triphenylmethyl-aziridinylmethanol

methyl N-trityl-L-serinate

(S)-methyl3-((methylsulfonyl)oxy)-2-(tritylamino)propanoate

Downstream raw materials:

(R)-2-(but-3-enyl)-1-tritylaziridine

(S)-2-(azidomethyl)-1-tritylaziridine

(R)-2-(4-chlorobenzyl)-1-tritylaziridine

(R)-2-benzyl-1-tritylaziridine