Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | (3-Aminobenzyl)diethylamine | HCID 3359246 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69456164 | HCID 69456164 | — |
Reaction Steps
1.00 g (9.99 mmol) Acetylacetone, 1.78 g (9.99 mmol) 3-[(diethylamino)methyl]-aniline, and 0.15 g (2.5 mmol) 4-toluenesulfonic acid are dissolved in 100 ml toluene. The reaction mixture is refluxed overnight with a Dean-Stark trap to remove water. 0.05 g (0.83 mmol) 4-toluenesulfonic acid are again added and the mixture is refluxed overnight. As tlc control showed that there is some 3-[(diethylamino)-methyl]aniline left, 0.2 g (2 mmol) acetylacetone are added and refluxing is continued for 4 h. To drive the reaction to completion, 0.6 ml (9.98 mmol) acetic acid and 0.2 g (2 mmol) acetylacetone are added and the mixture is refluxed overnight with a Dean-Stark trap. After cooling down to room temperature, the solvent is removed in vacuo and the residue is purified by column chromatography on silica with dichloromethane/methanol mixtures as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07199136B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-f56795cd69494eab86f45a0d8cac3ce2 |
|---|
| Source note | uspto-grants-2007_04 |
|---|