(2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

Base Information

Chemical Name:(2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine
CAS No.:420087-29-2
Molecular Formula:C₁₄H₂₃NO₂SSi
Molecular Weight:297.494
Hs Code.:

Synonyms:(2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

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

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Chemical Property of (2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

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Technology Process of (2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

There total 2 articles about (2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine 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: 7.0%

: 420087-33-8
(2R,3R)-2-methyl-3-phenylaziridine

: 106018-85-3
2-trimethylsilanyl-ethanesulfonyl chloride

: 420087-29-2
(2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

Guidance literature:: (2R,3R)-2-methyl-3-phenylaziridine; With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at -10 ℃; for 0.0833333h;

2-trimethylsilanyl-ethanesulfonyl chloride; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 873-66-5
1-propenylbenzene

: 106018-85-3
2-trimethylsilanyl-ethanesulfonyl chloride

: 420087-29-2
(2R,3R)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

: (2S,3S)-N-[2-(trimethylsilyl)ethanesulfonyl]-2-methyl-3-phenylaziridine

Guidance literature:: With pyridine N-oxide; [(R,R)-1,2-(N=CHC₆H₄O-o)2-cyclohexane]MnN; silver perchlorate; In pyridine; dichloromethane; at 0 ℃; for 12h; Title compound not separated from byproducts.;
DOI:10.1021/jo016146d