HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → HCID 18965748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 4-Methylbenzyl alcohol | HCID 11505 | — |
| Reactant | 4-Dodecylbenzenesulfonyl chloride | HCID 104215 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 18965748 | HCID 18965748 | 53% |
Reaction Steps
12.21 g (0.1 mol) of 4-methylbenzylalcohol was dissolved in 60 g of 1,4-dioxane, and was added while cooling to 11.22 g (0.1 mol) of potassium t-butoxide. The solution was added dropwise to a solution of 34.5 g (0.1 mol) of 4-dodecylbenzenesulfonyl chloride in 1,4-dioxane over one hour. Subsequently, 12.12 g (0.1 mol) of N,N-dimethylaniline was added and stirred at room temperature for 16 hours. After the completion of the reaction, the mixture was filtered and concentrated, and the precipitated solid was washed with ether and dried to give the titled compound. Yield: 53%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05349067 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-152854a4ed8d452baffab9c49ceeafac |
| Source note | uspto-grants-1994_09 |