HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 4-Hydroxy-4-methylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 8-Methyl-1,4-dioxaspiro(4.5)decan-8-ol | HCID 18713075 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxy-4-methylcyclohexanone | HCID 28539 | 86% |
Reaction Steps
To a solution of 8-methyl-1,4-dioxaspiro[4.5]decan-8-ol (1 equiv) in a 2:1 mixture of acetone and water (0.38 M) was added pyridinium p-toluenesulfonate (0.2 equiv). The resulting mixture was refluxed for 8 h. After the reaction was complete, the reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (0-30% ethyl acetate in petroleum ether) to afford the title compound (86% yield) as a yellow solid. 1H NMR (400 MHz, CHLOROFORM-d1) δ ppm 3.96-3.93 (m, 2H), 2.27-2.25 (m, 1H), 2.25-2.22 (m, 1H), 2.01-1.94 (m, 2H), 1.90-1.82 (m, 2H), 1.38 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428509B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b36d079ecd774d149cc24c9f0936d772 |
| Source note | uspto-grants-2016_08 |