HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
Reaction Steps
A rapidly stirring solution of the free base in ethyl acetate-ethanol or ethanol was treated with either p-toluenesulfonic acid monohydrate (1 equivalent; Aldrich; added as a solution in ethyl acetate) or HCl-dioxane (1-2 equivalent; 4 M; Aldrich) at room temperature. After stirring for 2-16 hours, the precipitate was collected by filtration, rinsed with ethyl acetate, and dried to afford the p-toluenesulfonate salt or the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163916B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-49d745850b5f40c6acaca3df35804352 |
| Source note | uspto-grants-2012_04 |