HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788971Generated: October 30, 2026
Hydrogen Peroxide → 4-Hydroxypiperazine-1-carbaldehyde
https://huagongshe.com/reaction/1788971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Ethoxycarbonylethyl-1-formylpiperazine | HCID 14399785 | — |
| Catalyst | Sodium Tungstate Dihydrate | HCID 150191 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxypiperazine-1-carbaldehyde | HCID 13937981 | — |
Reaction Steps
The crude 4-ethoxycarbonylethyl-1-formylpiperazine (114 g) prepared as described above is dissolved in water (500 ml) and sodium tungstate dihydrate (7.25 g) is added to the solution. At a temperature of 30°-35° C., 31% hydrogen peroxide (82 ml) is added dropwise to the solution and the mixture is stirred for one hour. The reaction mixture is stirred for 3 hours at room temperature and for another 5 hours at a temperature of 50°-55° C. The resulting reaction mixture is then shaken with ethyl acetate (300 ml). The aqueous layer is evaporated under reduced pressure to remove water to yield a dark brown oil. The oil is applied to a silica gel column chromatography for the purification (2 kg of silica gel, eluent; chloroform:methanol=10:1) and then is recrystallized from ethyl acetate to give 1-formyl-4-hydroxypiperazine (38.2 g), m.p. 118°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686221 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-328e456a645b482dab330921de96d6eb |
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| Source note | uspto-grants-1987_08 |
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