diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Base Information

Chemical Name:diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate
CAS No.:220586-52-7
Molecular Formula:C₁₉H₂₄NO₄PS
Molecular Weight:393.444
Hs Code.:

diethyl (S<sub>s</sub>,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Synonyms:diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Suppliers and Price of diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

There total 4 articles about diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate 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: 76.0%

: 220586-50-5
diethyl (S_s,1S,2R)-1-chloro-2-phenyl-2-(p-toluenesulfinamido)ethylphosphonate

: 220586-52-7
diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Guidance literature:: With sodium hydride;
DOI:10.1016/S0040-4039(98)02331-4

Reference yield:

: 3167-63-3
diethyl chloromethylphosphonate

: 220586-52-7
diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / LiHMDS / tetrahydrofuran; cyclohexane / 0.5 h / -78 °C

2: 76 percent / NaH / tetrahydrofuran; cyclohexane / 1 h / -78 - 20 °C

With sodium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; cyclohexane;
DOI:10.1021/jo020707z

Reference yield:

: 350479-90-2
(S,E)-N-benzylidene-4-methylbenzenesulfinamide

: 220586-52-7
diethyl (S_s,2S,3R)-(-)-N-(p-toluenesulfinyl)-3-phenylaziridine-2-phosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / LiHMDS / tetrahydrofuran; cyclohexane / 0.5 h / -78 °C

2: 76 percent / NaH / tetrahydrofuran; cyclohexane / 1 h / -78 - 20 °C

With sodium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; cyclohexane;
DOI:10.1021/jo020707z