HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)trimethylsilane → 1,3-Dimethyl-2-dimethylaminoimidazolidinium methylsulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)trimethylsilane | HCID 70454 | — |
| Reactant | 1,3-Dimethyl-2-chloroimidazolidinium methylsulfate | HCID 86613035 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1,3-Dimethyl-2-dimethylaminoimidazolidinium methylsulfate | HCID 86063873 | 85.7% |
Reaction Steps
1.33 g (11.34 mmol) of N,N-diethyltrimethylsilylamine are added over the course of 5 minutes at room temperature and with vigorous stirring to 2.50 g (10.22 mmol) of 1,3-dimethyl-2-chloroimidazolidinium methylsulfate in 10 ml of dry chloroform. The solvent is distilled off, and the residue is washed three times with 5 ml of diethyl ether and subsequently dried under a reduced pressure of 7.0 Pa and at 50° C. for 1 hour. The product is crystallised from a mixture of tetrahydrofuran:diethyl ether (1:1), giving 2.22 g of 1,3-dimethyl-2-dimethylaminoimidazolidinium methylsulfate, corresponding to a yield of 85.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439395B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-e276b8e455f548b9bc17de4f7ed3f01e |
| Source note | uspto-grants-2008_10 |