HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2-Acetyl-1,3-cyclohexanedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | 3-Acetoxy-2-cyclohexen-1-one | HCID 2755443 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2-Acetyl-1,3-cyclohexanedione | HCID 138104 | 59% |
Reaction Steps
According to Scheme 4 Step 2: AlCl3 (26.5 mmol, 3.53 g) was added to a solution of 3-oxocyclohex-1-enyl acetate (13.2 mmol, 2.04 g) in dichloroethane (10 mL) and the reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was poured onto a solution of H2SO4 in ice. The aqueous phase was extracted with CHCl3 (50 mL). The organic phase was washed with water, dried over Na2SO4, was filtered and was concentrated to yield 2-acetylcyclohexane-1,3-dione (7.78 mmol, 1.20 g, 59%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697744B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-411f976d5d964e97b0e5089fb4fd3785 |
| Source note | uspto-grants-2014_04 |