HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174513Generated: October 28, 2026
Formaldehyde → 1-(2-Hydroxyethyl)-4-methylpiperazine
https://huagongshe.com/reaction/1174513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Hydroxyethyl)-4-methylpiperazine | HCID 231184 | — |
Reaction Steps
In THF (30 ml) were added N-(2-hydroxyethyl)piperazine (500 mg, 3.84 mmol), a solution of formaldehyde (3117 mg, 38.41 mmol) and sodium cyanoborohydride (1207 mg, 19.20 mmol). The mixture was heated up to 50° C. overnight under stirring. After cooling some water was added and the mixture was extracted with DCM (3×). The organic layers were dried over MgSO4 and evaporated. The residue was purified over a silica plug with DCM/MeOH 9:1 as eluant to afford an oil (370 mg, Y=67%). 1H NMR (DMSO-d6) δ 4.45 (t, J=5.3 Hz, 1H), 3.51-3.45 (m, 2H), 3.02-2.84 (m, 4H), 2.71-2.64 (m, 2H), 2.61 (s, 3H), 2.58-2.53 (m, 2H), 2.47-2.43 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838522B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-fb44b903ea3d44e8a26aab9d8bf059fa |
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| Source note | uspto-grants-2010_11 |
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