HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679658Generated: October 30, 2026
Hydrochloric Acid → HCID 178517825, compound
https://huagongshe.com/reaction/1679658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Phenoxyethyl)hydrazine | HCID 20217 | — |
| Product | HCID 178517825 | HCID 178517825 | 43.8% |
Reaction Steps
30.4 g (0.2 mole) of 2-phenoxyethylhydrazine were dissolved in 200 ml of anhydrous acetonitrile and 7.3 g of hydrogen chloride gas were passed in at 0° C. 32 g (0.2 mole) of N-chlorocarbonyl-isocyanide-dichloride were then added dropwise to the mixture at 15°-20° C, while cooling and stirring vigorously, and after completion of the addition, 30 g of potassium carbonate were also added. The batch was next stirred for 4 hours at room temperature, in the course of which the temperature in the reaction vessel at times rose to as much as 45° C, and was then heated under reflux until no further evolution of hydrogen chloride was detectable (4-6 hours). After cooling, the residue was filtered off and washed with acetonitrile, and the total filtrate was evaporated under reduced pressure. The crystalline residue was recrystallized from a little ethanol. 21 g (43.8% of theory) of 1-(2-phenoxyethyl)-5-chloro-3-hydroxy-1,2,4-triazole of melting point 166° C were obtained. ##STR100##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04081535 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-c3a0a818aa454d1ba9ae32cdd076a56b |
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| Source note | uspto-grants-1978_03 |
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