HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1011866Erstellt: 27. Oktober 2026
1-Hexyne → 3,5-Diethyl-1-(3-hex-1-ynyl-phenyl)-1H-pyrazole-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/1011866
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Hexyne | HCID 12732 | — |
| Edukt | 1-(3-Bromo-phenyl)-3,5-diethyl-1H-pyrazole-4-carboxylic acid methyl ester | HCID 67313992 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Lösungsmittel | Piperidine | HCID 8082 | — |
| Produkt | 3,5-Diethyl-1-(3-hex-1-ynyl-phenyl)-1H-pyrazole-4-carboxylic acid methyl ester | HCID 67314187 | — |
Reaktionsschritte
A solution of 4.20 g (10.0 mmol) of 1-(3-bromo-phenyl)-3,5-diethyl-1H-pyrazole-4-carboxylic acid methyl ester (intermediate 1C) in 35 ml of piperidine was treated with 0.19 g (1.0 mmol) of copper(I)iodide and 1.16 g (1.0 mmol) of tetrakis-(triphenylphosphine)-palladium. The reaction mixture was warmed up to 60° C. and after 15 min, a solution of 0.82 g=1.00 ml (10.0 mmol) of hex-1-yne in 15 ml of piperidine was added drop by drop during 1 hour. After 30 min, the oil bath temperature was steadily increased to 80° C. The reaction mixture was then stirred at 80° C. for 4 hours, and subsequently cooled down to RT. The solvent was evaporated and the residue poured into crashed ice, acidified with HCl (37%) to pH 1-2 and extracted twice with EtOAc; the organic phases were washed with water, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography (n-heptane:EtOAc 1:0-9:1) to afford the title compound as light yellow oil. MS: 339.0 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07977358B2 |
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| Quelldatensatz | uspto-grants-2011_07 |
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| ORD ID | ord-136b20bce9594ee99e6b6b12daba7ba8 |
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| Quellennotiz | uspto-grants-2011_07 |
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