HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784656Generated: October 25, 2026
Ethylenediamine → 2-(4-methoxyphenyl)piperazine
https://huagongshe.com/reaction/1784656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | (4-Methoxyphenyl)glyoxal | HCID 70643 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-methoxyphenyl)piperazine | HCID 2771753 | 45.3% |
Reaction Steps
Methanol (5 ml) solution of ethylenediamine (3.74 g, 62.29 mmol) was added to the ice-cooled solution of 4-methoxyphenylglyoxal (8.30 g, 45.5 mmol) in methanol (100 ml) and tetrahydrofuran (50 ml) and stirred for 10 min. After cooling to 0° C., sodium tetrahydroborate (6.14 g, 162.2 mmol) and additional methanol (50 ml) was added and stirred overnight. After removal of the solvent, aqueous sodium hydroxide was added and was extracted with dichloromethane three times and washed with brine and dried over sodium sulfate. After removal of the solvent, purification of the residue by silica gel column chromatography (eluent; dichloromethane/ethanol/diethylamine=20/2/1) gave 2-(4-methoxypheny)-piperazine (3.96 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504411B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-1bb930f324334d69b46eb823f018c576 |
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| Source note | uspto-grants-2009_03 |
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