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Merck

902624

Sigma-Aldrich

Diethyl 2-((tosyloxy)imino)malonate

≥95%

别名:

Kurti doubly N-electrophilic iminomalonate

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About This Item

经验公式(希尔记法):
C14H17NO7S
CAS号:
分子量:
343.35
分類程式碼代碼:
12352202

化驗

≥95%

形狀

powder or crystals

存貨情形

available only in USA

mp

63-66 °C

應用

As demonstrated by Laszlo Kürti′s lab, ketomalonate oxime O-sulfonates act as doubly N-electrophilic linchpin reagents towards strong C-nucleophiles such as alkyl- and arylmetals (e.g., Grignard reagents). Thus, symmetrical dialkyl- as well as diarylamines may be directly prepared at low tempretatures and in the absence of transition metal catalysts. Other ketomalonate oxime O-sulfonates include 902918, 902705 and 902748.

象形圖

Flame

訊號詞

Danger

危險聲明

危險分類

Self-react. C

儲存類別代碼

5.2 - Organic peroxides and self-reacting hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Highly efficient sequential N,N,C-trialkylation of α-N-acyloxyimino esters.
Mizota I, et al.
Tetrahedron, 71, 5793-5799 (2015)
Aneta Bogdanova et al.
Journal of the American Chemical Society, 126(36), 11293-11302 (2004-09-10)
The photochemical or thermal decomposition of ethyl diazomalonate (1) or ethyl 3,3-diazirinedicarboxylate in methanol solutions yields the O-H insertion product 6, while products of the Wolff rearrangement were not detected in both cases. The analysis of temperature-dependent (13)C NMR spectra
Padmanabha V Kattamuri et al.
Journal of the American Chemical Society, 139(32), 11184-11196 (2017-06-27)
Given the importance of amines in a large number of biologically active natural products, active pharmaceutical ingredients, agrochemicals, and functional materials, the development of efficient C-N bond-forming methods with wide substrate scope continues to be at the frontier of research

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