HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Isopropylcyclohexan-1-ol → 2-Isopropylcyclohexan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Isopropylcyclohexan-1-ol | HCID 95331 | — |
| Reactant | HCID 178526115 | HCID 178526115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isopropylcyclohexan-1-one | HCID 70490 | — |
Reaction Steps
To a suspension of 4.0 g. (13.7 mmole) of 2,2'-bipyridinium chlorochromate in 15 ml of dichloromethane is added, while stirring, 0.5 g. (3.5 mmole) of 2-isopropylcyclohexanol in 10 ml of dichloromethane. The resulting reaction mixture is stirred for 4 hours and then filtered through a Hirsch funnel packed with 2 cm of Celite®. The resulting clear filtrate is washed with 5% hydrochloric acid and 10% sodium carbonate, and dried over magnesium sulfate. The drying agent is then removed and the solvent evaporated to yield a colorless oil which is distilled via Kugelrohr to yield pure 2-isopropylcyclohexanone in a typical yield of 0.425 g. which is 86% of theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04399281 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-202a73537e6b474f91ffe9d816766776 |
| Source note | uspto-grants-1983_08 |