A practical route to 1-(6-chloropyridazin-3-yl)-3(5)-aryl-5(3)-trifluoromethylpyrazoles using Aliquat 336

The objective of the study is to simplify the synthetic strategy for the synthesis of 1-(6-chloropyridazin-3-yl)-3(5)-aryl-5(3)-trifluoromethylpyrazoles. An elaborated literature survey has been reported by us which documents several routes for the synthesis of 3(5)-trifluoromethylpyrazoles, but none of the methods involves the synthesis of 3(5)-trifluoromethylpyrazoles utilising the Aliquat 336 catalyst21. So, the present study has been undertaken to explore the new synthetic routes. Route A: One-pot synthesis of 1-(6-chloropyridazin-3-yl)-3-aryl-5-trifluoromethylpyrazoles 5(b-e) was undertaken via refluxing 3-chloro-6-hydrazinopyridazine 2 with 4,4,4-trifluoro-1-phenylbutane-1,3-dione 1(b-e) under anhydrous methanol for 2h. Later, in situ addition of 4-5 drops of sulphuric acid (concentrated) to the reaction mixture was carried out, and it was boiled for 1h till the completion of the reaction. Meticulously, condensation of 3-chloro-6-hydrazinopyridazine 2 along with trifluoromethylacetylacetone 1a was carried out under anhydrous methanol refluxing conditions for 2 h and resulted in the exclusive formation of 5-trifluoromethylpyrazoles 5a. Route B: Further, Aliquat 336-catalyzed regioselective synthesis of 1-(6-chloropyridazin-3-yl)-5-aryl-3-trifluoromethylpyrazoles 6(b-e) was carried out, without the major side products formation, via stirring 3,6-dichloropyridazine 9 with 3(5)-trifluoromethyl-5(3)-substituted-1H-pyrazoles 10 using the Aliquat 336 catalyst along with NaOH like a base under toluene reflux for 1h. Interestingly, the condensation of 2 with 2-thienyltrifluoromethyl-β-diketone 1f resulted in the exclusive formation of 3-trifluoromethylpyrazoles 6a. Tetra-alkylammonium ions (R4N+) obtained from Aliquat 336 i.e., Tetra-alkylammonium salts (R4N+X¯) have an unique property. They are soluble in aqueous medium due to their ionic nature but, at the same time, they are also soluble in non-polar organic solvents such as toluene, DCM due to the presence of four alkyl groups. Hence, tetra-alkylammonium ions (R4N+) are able to move back and forth between two phases. So, Aliquat 336 act as a phase transfer catalyst as it carries the inorganic anion such as ¯OH which is insoluble in toluene. Hence, ¯OH ion helps in generating the anion of 3(5)-trifluoromethyl-5(3)-substituted-1H-pyrazoles in organic phase and the anion attacks the target compound 3,6-dichloropyridazine to replace the Cl¯ group. The structure of all the synthesized candidates were reasonably characterized with the analysis of ^1H, ^13C, and ^19F-NMR spectroscopy. Route A: provides easy handling and improved yield. Route B provides easily accessible way without the formation of side products.

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Journal
Discover Chemistry.
Published
2026-10-29
DOI
https://doi.org/10.1007/s44371-026-01035-3
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

A practical route to 1-(6-chloropyridazin-3-yl)-3(5)-aryl-5(3)-trifluoromethylpyrazoles using Aliquat 336

Ranjana Aggarwal, Swati Sharma
Discover Chemistry.
Fluorine in Organic Chemistry
article

A practical route to 1-(6-chloropyridazin-3-yl)-3(5)-aryl-5(3)-trifluoromethylpyrazoles using Aliquat 336

Ranjana Aggarwal, Swati Sharma
article en

Abstract

The objective of the study is to simplify the synthetic strategy for the synthesis of 1-(6-chloropyridazin-3-yl)-3(5)-aryl-5(3)-trifluoromethylpyrazoles. An elaborated literature survey has been reported by us which documents several routes for the synthesis of 3(5)-trifluoromethylpyrazoles, but none of the methods involves the synthesis of 3(5)-trifluoromethylpyrazoles utilising the Aliquat 336 catalyst21. So, the present study has been undertaken to explore the new synthetic routes. Route A: One-pot synthesis of 1-(6-chloropyridazin-3-yl)-3-aryl-5-trifluoromethylpyrazoles 5(b-e) was undertaken via refluxing 3-chloro-6-hydrazinopyridazine 2 with 4,4,4-trifluoro-1-phenylbutane-1,3-dione 1(b-e) under anhydrous methanol for 2h. Later, in situ addition of 4-5 drops of sulphuric acid (concentrated) to the reaction mixture was carried out, and it was boiled for 1h till the completion of the reaction. Meticulously, condensation of 3-chloro-6-hydrazinopyridazine 2 along with trifluoromethylacetylacetone 1a was carried out under anhydrous methanol refluxing conditions for 2 h and resulted in the exclusive formation of 5-trifluoromethylpyrazoles 5a. Route B: Further, Aliquat 336-catalyzed regioselective synthesis of 1-(6-chloropyridazin-3-yl)-5-aryl-3-trifluoromethylpyrazoles 6(b-e) was carried out, without the major side products formation, via stirring 3,6-dichloropyridazine 9 with 3(5)-trifluoromethyl-5(3)-substituted-1H-pyrazoles 10 using the Aliquat 336 catalyst along with NaOH like a base under toluene reflux for 1h. Interestingly, the condensation of 2 with 2-thienyltrifluoromethyl-β-diketone 1f resulted in the exclusive formation of 3-trifluoromethylpyrazoles 6a. Tetra-alkylammonium ions (R4N+) obtained from Aliquat 336 i.e., Tetra-alkylammonium salts (R4N+X¯) have an unique property. They are soluble in aqueous medium due to their ionic nature but, at the same time, they are also soluble in non-polar organic solvents such as toluene, DCM due to the presence of four alkyl groups. Hence, tetra-alkylammonium ions (R4N+) are able to move back and forth between two phases. So, Aliquat 336 act as a phase transfer catalyst as it carries the inorganic anion such as ¯OH which is insoluble in toluene. Hence, ¯OH ion helps in generating the anion of 3(5)-trifluoromethyl-5(3)-substituted-1H-pyrazoles in organic phase and the anion attacks the target compound 3,6-dichloropyridazine to replace the Cl¯ group. The structure of all the synthesized candidates were reasonably characterized with the analysis of ^1H, ^13C, and ^19F-NMR spectroscopy. Route A: provides easy handling and improved yield. Route B provides easily accessible way without the formation of side products.

Discover Chemistry.Vol. 3(1)
Baba Mastnath University (IN), Council of Scientific and Industrial Research (IN)
University Grants Commission, Kurukshetra University
Openalex Percentile: Top 15%
Fluorine in Organic Chemistry
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