HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979049Generated: October 29, 2026
Tetrahydrofuran → HCID 20201642, compound
https://huagongshe.com/reaction/979049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | HCID 11062732 | HCID 11062732 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20201642 | HCID 20201642 | 49.7% |
Reaction Steps
Into 600 ml of tetrahydrofuran, were dissolved 41 g of 1-formylpiperazine and 54.5 g of triethylamine. To the solution, while being stirred and cooled in ice, was added dropwise 56 g of 2,4,4-trimethylallophanyl chloride. The mixture was allowed to react at room temperature for 6 hours and the precipitate was removed by filtration. The filtrate was concentrated and the residue was recrystallized from tetrahydrofuran to obtain 41 g of 1-formyl-4-(2,4,4-trimethylallophanoyl)piperazine. This compound was mixed with 800 ml of 6N hydrochloric acid and the mixture was heated with stirring at 60° C. for one hour. The reaction mixture was concentrated and the residue was recrystallized from ethanol to obtain 35.2 g of 1-(2,4,4-trimethylallophanoyl)piperazine hydrochloride having a melting point of 215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04666911 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-3ea879f65a1147f0a895e0e711a967d8 |
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| Source note | uspto-grants-1987_05 |
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