HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Amino-1,3-bis[[p-(dimethylamino)benzylidene]amino]imidazolium tetrafluoroborate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1,3-Bis[[p-(dimethylamino)benzylidene]amino]-2-(methylthio)imidazolium tetrafluoroborate | HCID 73867526 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-1,3-bis[[p-(dimethylamino)benzylidene]amino]imidazolium tetrafluoroborate | HCID 73867531 | — |
Reaction Steps
0.99 g of 1,3-bis[[p-(dimethylamino)benzylidene]amino]-2-(methylthio)imidazolium tetrafluoroborate is dissolved in 15 ml of absolute dimethylformamide. Dry ammonia is conducted into the reaction solution at room temperature while stirring until the cleavage of methyl mercaptan is complete. The solution is treated with diethyl ether. The precipitate obtained is washed twice with water and twice and cold methanol and re-precipitated from dimethylformamide/diethyl ether. There is obtained yellow 2-amino-1,3-bis[[p-(dimethylamino)benzylidene]amino]imidazolium tetrafluoroborate with a decomposition point >260°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814332 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-ddbdacf00e8d4edcb9475339aca3359f |
| Source note | uspto-grants-1989_03 |