4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

Base Information

Chemical Name:4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one
CAS No.:130065-00-8
Molecular Formula:C₁₇H₂₅N₃O₅Si
Molecular Weight:379.488
Hs Code.:

Synonyms:4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

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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 4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

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Technology Process of 4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

There total 2 articles about 4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one 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: 73.0%

: 2-(Trimethylsilyl)ethyl azidoformate

: 130064-91-4
4-Methyl-1-(o-nitrobenzyl)pyrazolidin-3-one

: 130065-00-8
4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

Guidance literature:: With sodium hydride; In tetrahydrofuran; 1) 0 deg C, 30 min, 2) r.t., 1.5 h;
DOI:10.1021/jo00311a023

Reference yield:

: 612-23-7
2-nitrobenzyl chloride

: 130065-00-8
4-Methyl-1-(o-nitrobenzyl)-2-<2-(trimethylsilyl)ethoxycarbonyl>pyrazolidin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / Et₃N, NaI / dimethylformamide / 48 h / Ambient temperature

2: 73 percent / 60percent NaH / tetrahydrofuran / 1) 0 deg C, 30 min, 2) r.t., 1.5 h

With sodium hydride; triethylamine; sodium iodide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo00311a023