HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1H-Pyrrole-2-methanaminium, N,N,N-trimethyl-, iodide (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | dimethyl[(1H-pyrrol-2-yl)methyl]amine | HCID 260796 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1H-Pyrrole-2-methanaminium, N,N,N-trimethyl-, iodide (1:1) | HCID 13975138 | — |
Reaction Steps
To a cold solution of 67 g (0.47 mole) of methyliodide in 150 ml of anhydrous ether was added slowly a dry ether solution of 50 gm of 2-(N,N-dimethylaminomethyl)pyrrole (0.37 mole). A white solid begain to precipitate out of solution. The mixture was heated to 30° for 1.5 hours, filtered and washed with 2/×30 ml of ether to obtain 59 gm of 2-pyrryl)methyltrimethylammonium iodide which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04746669 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-c27057f2bf954469bd09079bd76b3332 |
| Source note | uspto-grants-1988_05 |