HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → HCID 73867527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 73867529 | HCID 73867529 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 73867527 | HCID 73867527 | — |
Reaction Steps
4.1 g of 1,3-bis(benzylideneamino)-2-(methylthio)imidazolium tetrafluoroborate in 25 ml of absolute acetonitrile are treated under an argon atmosphere with 1.45 g of absolute morpholine, whereby the evolution of methylmercaptan sets in immediately and solution occurs. The solution is left to stir overnight at room temperature until the cleavage of methylmercaptan is complete. The resulting colorless precipitate is removed by filtration. The filtrate is treated with 30 ml of diethyl ether and again filtered. The two filter residues are combined and reprecipitated from acetonitrile/ether. There is obtained 1,3-bis(benzylideneamino)-2-morpholinoimidazolium tetrafluoroborate in the form of colorless crystals of m.p. 244°-247° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908363 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-c2176249c50b415596fe020bc956e950 |
| Source note | uspto-grants-1990_03 |