HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604556Generated: October 26, 2026
Formaldehyde → 1-(1-Ethyl-1H-pyrrol-2-yl)-N,N-dimethylmethanamine
https://huagongshe.com/reaction/604556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Ethylpyrrole | HCID 185226 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(1-Ethyl-1H-pyrrol-2-yl)-N,N-dimethylmethanamine | HCID 45088335 | 97% |
Reaction Steps
A mixture of a 35% aqueous formaldehyde solution (9.0 mL, 105 mmol) and dimethylamine hydrochloride (9.0 g, 110 mmol) was added to 1-ethylpyrrol (10.0 g, 105 mmol) under ice-cooling with stirring over 1 hour and 30 minutes and the mixture was stirred at room temperature for 6 hours. A 10% aqueous sodium hydroxide solution (150 mL) and ether were added to the reaction mixture to separate it. The thus obtained organic phase was separated, washed with a saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography (methylene chloride:methanol, 9:1) to obtain 2-(N,N-dimethylaminomethyl)-1-ethylpyrrol (15.6 9, yield: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910617B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-eb81db39084e4ab794d972745fa2042f |
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| Source note | uspto-grants-2011_03 |
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