Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 2-butyl-1H-imidazole | HCID 11815351 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178443872 | HCID 178443872 | — |
Reaction Steps
In a 250 ml Schlenk flask, 48.04 g (0.381 moles) of dimethyl sulfate was slowly added dropwise to 47.31 g (0.381 moles) of butylimidazole with ice cooling and under a blanket gas. Stirring of the mixture was continued at room temperature over night. After the addition of 62.72 g (0.482 moles; 1.26 equ.) of 1-octanol and 0.67 g of Dowex ion-exchanger washed with acetone and dried under high vacuum, the mixture was allowed to react over night at 140° C., and at the same time, the by-product methanol formed was removed from the reaction mixture by sparging with an argon stream. The remaining volatile fractions were subsequently removed under high vacuum at 80° C. The product, 1-butyl-3-methylimidazolium 1-octyl sulfate, was obtained as a viscous, slightly yellow liquid in quantitative yield. The product does not contain any detectable amounts of Cl− contamination (AgNO3 test; <3 ppm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07655803B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-218402e4a71a463f810bb19150e54d1a |
|---|
| Source note | uspto-grants-2010_02 |
|---|