Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 86739431 | HCID 86739431 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57034955 | HCID 57034955 | 72% |
Reaction Steps
320 ml of concentrated sulphuric acid and 94 ml of water were added to 266.3 g of 1-cyano-1-(3-trifluoromethylphenyl)-3-(1,2,4-triazol-l-yl)-propanone hydrochloride, and the mixture was heated at 100° C. for 1.5 hours. After the vigorous evolution of CO2 had ended, the mixture was allowed to cool, and 940 ml of water were added. After a short time at from 0° to 20° C., the sulphate of the desired end product crystallized out. This was suspended in water, and the suspension was adjusted to a pH value of 7-8 with sodium bicarbonate solution. The resulting crystalline precipitate was filtered off under suction, dissolved in chloroform, dried over sodium sulphate and concentrated. 131.3 g (72% of theory) of 1-(3-trifluoromethylphenyl)-3-(1,2,4-triazol-l-yl)-propanone of melting point 85° to 87° C. were obtained. ##STR8##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04451282 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-e18c4cfaf2f04316860703fdbb387048 |
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| Source note | uspto-grants-1984_05 |
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