HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254189Generated: October 31, 2026
Formaldehyde → 3-[(4-methylpiperazin-1-yl)methyl]-1H-indole
https://huagongshe.com/reaction/254189
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Indole | HCID 798 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(4-methylpiperazin-1-yl)methyl]-1H-indole | HCID 227584 | — |
Reaction Steps
In a three necked round bottom flask equipped with pressure equalizing funnel, indole (1.17 g, 0.01 mole) and dichloromethane (8 mL) were taken. 1-Methylpiperazine (1.01 g, 0.011 moles) and formaldehyde (9 mL, 0.012 mole) was added slowly at room temperature and the reaction mixture was stirred well for one hour. After the completion of reaction (TLC), the product was isolated by distillation under reduced pressure. The residue was extracted with ethyl acetate (2×25 mL). The combined organic extracts were washed with water, followed by brine, dried over anhydrous sodium sulfate. The organic layer was evaporated under vacuum. The residue could either be an oily liquid or solid mass. The oily mass was triturated with n-hexane to obtain a solid material. The solid obtained was identified by IR, NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875605B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-f91cdf5d70774916aca3c0f30b8af2e5 |
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| Source note | uspto-grants-2011_01 |
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