HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568973Generated: October 30, 2026
Hydrochloric Acid → HCID 20149487, compound
https://huagongshe.com/reaction/568973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20149438 | HCID 20149438 | — |
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Reactant | Dioxan ethanol | HCID 22560076 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20149487 | HCID 20149487 | — |
Reaction Steps
The foregoing compound 22 (17.5 g, 31.8 mmoles) and a 1M solution of N2H4.H2O in dioxane/ethanol 4:1 (35 mL, 2 equivalents) are stirred and heated at about 90° C. After 3 hours, a yellow precipitate is formed, and the mixture is allowed to cool to room temperature. The precipitate is filtered and the filtrate is evaporated to yield an oil. The oil and the precipitate are united and heated with ethanol (310 mL) and conc. HCl (18.6 mL) at 90° C. for 3 hours. After cooling, phthalhydrazide is filtered and the solution is evaporated. Dissolving in water, filtration, evaporation, dissolving in ethanol, evaporating again and drying (oil pump) yields a yellow foam: 11.5 g (about 100%). Thin layer chromatography (ethanol/ammonia 80/20) shows a second spot (presumably some ester cleaved). The compound 23 is utilized for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04730006 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-855a897586584be5a0c309f2878ebce1 |
|---|
| Source note | uspto-grants-1988_03 |
|---|