HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (1-Ethylpyrrol-2-yl)methyltrimethylammonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(1-Ethyl-1H-pyrrol-2-yl)-N,N-dimethylmethanamine | HCID 45088335 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1-Ethylpyrrol-2-yl)methyltrimethylammonium iodide | HCID 23031652 | 66% |
Reaction Steps
Methyl iodide (7.7 mL, 124 mmol) was added to a solution of 2-(N,N-dimethylaminomethyl)-1-ethylpyrrol (15.6 g, 102 mmol) in ethanol (150 mL) under ice-cooling and the mixture was stirred at room temperature for 3 hours. Ethyl acetate (150 mL) was added to the reaction mixture and the precipitated crystal was collected by filtration. After the crystal was washed with ethyl acetate and dried to obtain (1-ethylpyrrol-2-yl)methyltrimethylammonium iodide (20.0 g, yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910617B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-4a6674ca47a74df7a8c542caf9559112 |
| Source note | uspto-grants-2011_03 |