HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295997Generated: October 27, 2026
1H-1,2,4-Triazole → 4-Fluoro-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one
https://huagongshe.com/reaction/2295997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-3,3-dimethyl-4-fluoro-2-butanone | HCID 13019442 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Fluoro-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one | HCID 12769539 | 60.5% |
Reaction Steps
197 g (1 mole) of 1-bromo-3,3-dimethyl-4-fluoro-2-butanone were slowly added dropwise to a boiling solution of 77 g (1.1 mols) of 1,2,4-triazole and 210 g (1.5 moles) of potassium carbonate in 500 ml of acetone such that, after removing the heating bath, the exothermic reaction kept the solution simmering. The mixture was then kept under reflux for a further 3 hours, the inorganic salts were filtered off and the filtrate was concentrated in vacuo. The residue was taken up in chloroform/water and the organic phase was separated off and evaporated. The residue which remained was distilled in vacuo and the distillate was crystallized with cyclohexane. 112 g (55% of theory) of 3,3-dimethyl-4-fluoro-1-(1,2,4-triazol-1-yl)-butan-2-one of melting point 59° C. were obtained. ##STR15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04427672 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-3f559018a0e2471697e58107e3058f3c |
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| Source note | uspto-grants-1984_01 |
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