HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382151Generated: October 30, 2026
Potassium Carbonate → HCID 14392496, compound
https://huagongshe.com/reaction/1382151
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Reactant | HCID 21274223 | HCID 21274223 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 14392496 | HCID 14392496 | 93.9% |
Reaction Steps
A mixture of 0.56 g (0.0019 mole) of 1-(2,4-dichloro-5-hydroxyphenyl)-4-fluoromethyl-4,5-dihydro-3-methyl-1,2,4-triazol-5(1H)-one and 1.1 g (0.0076 mole) of anhydrous potassium carbonate in 15 mL of acetone was stirred for 15 minutes. Sodium iodide (approximately 0.01 g) and 0.37 g (0.002 mole) of ethyl 2-bromopropionate were added, and the resultant mixture was heated at reflux for 1.5 hours. The mixture was cooled and filtered. The filtrate was evaporated under reduced pressure, leaving a residue. This residue was partitioned between diethyl ether and water. The organic phase was washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated under reduced pressure, leaving an oil. This oil was stirred in n-pentane, and the supernant was decanted, leaving an oily residue. The oil was dried at 70° C. under a stream of nitrogen to yield 0.70 g of ethyl 2-[2,4-dichloro-5-(4-fluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenoxy]propionate, Compound 13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04806145 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-58f447b2eba8491abc6bd52b7f54368a |
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| Source note | uspto-grants-1989_02 |
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