HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethyl-2-methyl-1,3-benzothiazol-3-ium bromide → 3-Ethyl-2-methylbenzothiazolium tetracyanoborate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethyl-2-methyl-1,3-benzothiazol-3-ium bromide | HCID 12859978 | — |
| Reactant | Potassium Tetracyanoborate | HCID 23686396 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-2-methylbenzothiazolium tetracyanoborate | HCID 86624469 | 89.1% |
Reaction Steps
1.64 g (10.66 mmol) of potassium tetracyanoborate, K[B(CN)4], in 5 ml of water are added dropwise with stirring to a solution of 2.76 g (10.69 mmol) of 3-ethyl-2-methylbenzothiazolium bromide in 50 ml of water. The lower liquid phase is extracted a number of times with 50 ml of dichloromethane, and the combined organic phases are dried using Mg2SO4. The solvent is subsequently removed by distillation, and the residue is dried under a reduced pressure of 1.3 Pa and at 60° C., giving 2.78 g of 3-ethyl-2-methylbenzothiazolium tetracyanoborate, corresponding to a yield of 89.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939644B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-fa02857ed4be4dbaa5305a448548728b |
| Source note | uspto-grants-2011_05 |