HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 2-Ethylcyclohexane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Hantzsch ester | HCID 70849 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Ethylcyclohexane-1,3-dione | HCID 10898805 | 69% |
Reaction Steps
1,3-Cyclohexanedione (10 g, 89.2 mmol), 40% aqueous CH3CHO (49.4 g, 445.9 mmol) were dissolved in methanol (40 mL) followed by addition of Hantzsch ester (22.7 g, 89.2 mmol) and pyridine (2.1 g, 18.74 mmol) under nitrogen. The resulting light yellow mixture was stirred at room temperature overnight, then concentrated to give crude product that was re-slurried in a mixture of CH2Cl2 (40 mL) and hexanes (60 mL) to furnish 2-ethyl-1,3-cyclohexanedione (8.6 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073888B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-0be1b85333fe4f2e857f2598abcd2658 |
| Source note | uspto-grants-2015_07 |