HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422941Generated: October 29, 2026
Formaldehyde → N,N-dimethyl-1-(1H-pyrrol-2-yl)methanamine
https://huagongshe.com/reaction/422941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | N,N-dimethyl-1-(1H-pyrrol-2-yl)methanamine | HCID 260796 | 90.5% |
Reaction Steps
A mixture of 35% aqueous formaldehyde solution (3.2 ml, 40.7 mmol) and dimethylamine hydrochloride (3.44 g, 42.4 mmol) was added to pyrrole (2.72 g, 40.47 mmol) at room temperature with stirring over a 20-minute interval, and the resulting mixture was stirred at room temperature for 2 hours. After stirring, 10% aqueous sodium hydroxide solution (18 ml) was added to the reaction mixture, and the reaction mixture was extracted with dichloromethane. The extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After filtration, the solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (10:1) as the eluent to afford 2-(N,N-dimethylaminomethyl)pyrrole (4.55 g, quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101650B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c9c061f5073f415aab32425d07acee14 |
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| Source note | uspto-grants-2012_01 |
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