HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018447Generated: October 25, 2026
Formaldehyde → 1-Ethyl-4-(hydroxymethyl)piperazine-2,3-dione
https://huagongshe.com/reaction/1018447
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-Ethyl-2,3-piperazinedione | HCID 108812 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-Ethyl-4-(hydroxymethyl)piperazine-2,3-dione | HCID 18401456 | 100% |
Reaction Steps
To a solution of 1-ethylpiperazine-2,3-dione (2.13 g, 15 mmol) in 30% aqueous (methanol free) formaldehyde (15 mmol) potassium hydroxide (150 mg, 2.7 mmol) was added and the mixture stirred at 50° C. for 7 days. It was neutralized with 5 N aqueous hydrochloric acid (50 μl) to pH=7. The mixture was evaporated at 15 mm and then dried in high vacuo (0.0013 mbar) (0.001 mm) to give 1-ethyl-4- (hydroxymethyl)-piperazine-2,3-dione as a colourless solid (100%). NMR-spectrum in CDCl3: 1.15 (broad signal, 1H), 1.15 (t, 3H, J=7 Hz), 3.47 (q, 2H, J=7 Hz), 3.54 (m, 2H), 3.68 (m, 2H), 4.88 (s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482818B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-1896bacf1ee24ef1b74871aae3e5d2e0 |
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| Source note | uspto-grants-2002_11 |
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