HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 20512424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 2-Imidazolidinimine, 1,3-bis(2,6-dimethylphenyl)- | HCID 11204080 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20512424 | HCID 20512424 | 82.4% |
Reaction Steps
A mixture of 8.3 g (28.3 mmoles) of 1,3-bis(2',6'-dimethylphenyl)-2-imino-imidazolidine, prepared as described in Example 1, Method (a), 150 ml of methyl-ethyl-ketone, 10.0 g (0.1 moles) of potassium hydrogencarbonate and 1.85 ml (4.26 g, 30 mmoles) of methyl iodide is stirred at room temperature for 8 hours. The separated precipitate is filtered off, and the filtrate is evaporated in vacuo. The residue is combined with the precipitate obtained with the previous operation, suspended in 150 ml of water, allowed to stand for 2 hours, and then the insolubles are filtered off. 10.15 g (82.4%) of crude 1,3-bis(2',6'-dimethylphenyl)-2-methylimino-imidazolidine hydroiodide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369325 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-6bff46c2925f4e26a1c79751400a59ce |
| Source note | uspto-grants-1983_01 |