Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dodecylbenzenesulphonic acid | HCID 25457 | — |
| Reactant | Dimedone | HCID 31358 | — |
| Reactant | (3-Formyl-4-methoxyphenyl)boronic acid | HCID 2759225 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131732562 | HCID 131732562 | 64% |
Reaction Steps
(3-Formyl-4-methoxyphenyl)boronic acid (5.30 g, 29.5 mmol) and 5,5-dimethylcyclohexane-1,3-dione (8.26 g, 58.9 mmol) were added to a suspension of dodecylbenzenesulfonic acid (0.96 g, 2.94 mmol) in water (196 ml) at room temperature, and the mixture thus obtained was then stirred under heating to reflux for 5 hours. After air-cooling, a solid was collected from the reaction solution by filtration. The solid thus obtained was suspended in ethanol, and the solution thus obtained was then stirred under heating to reflux. After air-cooling, the solvent was distilled away from the reaction solution under reduced pressure. Diethyl ether was added to the residue thus obtained, and the solid thus generated was collected by filtration and was then dried to obtain the title compound (7.99 g, yield: 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08975263B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-fd19bbf8aa1449699f9f22bc48134c02 |
|---|
| Source note | uspto-grants-2015_03 |
|---|