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Pregled bibliografske jedinice broj: 1183720

1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles


Opsomer, Tomas; Valkeneers, Kaat; Ratković, Ana; Dehaen, Wim
1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles // Organics, 2 (2021), 404-414 doi:10.3390/org2040024 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1183720 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles

Autori
Opsomer, Tomas ; Valkeneers, Kaat ; Ratković, Ana ; Dehaen, Wim

Izvornik
Organics (2673-401X) 2 (2021); 404-414

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
1, 2, 3-triazole ; aldehyde ; cycloaddition ; enamine ; Cornforth ; rearrangement ; amines ; metal-free

Sažetak
1, 2, 3-Triazole-4-carbaldehydes are useful synthetic intermediates which may play an important role in the discovery of novel applications of the 1, 2, 3-triazole moiety. In this work, a one-step multigram scale synthesis of 4- formyl-1-(4-nitrophenyl)-1H-1, 2, 3-triazole (FNPT) as a preferred reagent for the synthesis of 1- alkyl-4-formyltriazoles is described, making use of the commercially available 3- dimethylaminoacrolein and 4-nitrophenyl azide. Next, the earlier reported reaction of FNPT with alkylamines is further explored, and for hexylamine, the one-pot sequential cycloaddition and Cornforth rearrangement is demonstrated. In addition, a useful protocol for the in situ diazotization of 4-nitroaniline is provided. This facilitated the complete hydrolysis of rearranged 4-iminomethyl- 1, 2, 3-triazoles and allowed for the recycling of 4-nitrophenyl azide.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Fidelta d.o.o.

Profili:

Avatar Url Ana Grgičević (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Opsomer, Tomas; Valkeneers, Kaat; Ratković, Ana; Dehaen, Wim
1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles // Organics, 2 (2021), 404-414 doi:10.3390/org2040024 (međunarodna recenzija, članak, znanstveni)
Opsomer, T., Valkeneers, K., Ratković, A. & Dehaen, W. (2021) 1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles. Organics, 2, 404-414 doi:10.3390/org2040024.
@article{article, author = {Opsomer, Tomas and Valkeneers, Kaat and Ratkovi\'{c}, Ana and Dehaen, Wim}, year = {2021}, pages = {404-414}, DOI = {10.3390/org2040024}, keywords = {1, 2, 3-triazole, aldehyde, cycloaddition, enamine, Cornforth, rearrangement, amines, metal-free}, journal = {Organics}, doi = {10.3390/org2040024}, volume = {2}, issn = {2673-401X}, title = {1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles}, keyword = {1, 2, 3-triazole, aldehyde, cycloaddition, enamine, Cornforth, rearrangement, amines, metal-free} }
@article{article, author = {Opsomer, Tomas and Valkeneers, Kaat and Ratkovi\'{c}, Ana and Dehaen, Wim}, year = {2021}, pages = {404-414}, DOI = {10.3390/org2040024}, keywords = {1, 2, 3-triazole, aldehyde, cycloaddition, enamine, Cornforth, rearrangement, amines, metal-free}, journal = {Organics}, doi = {10.3390/org2040024}, volume = {2}, issn = {2673-401X}, title = {1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4- carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles}, keyword = {1, 2, 3-triazole, aldehyde, cycloaddition, enamine, Cornforth, rearrangement, amines, metal-free} }

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