HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → Cyclohexanone, 2-(2-ethoxyethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Product | Cyclohexanone, 2-(2-ethoxyethyl)- | HCID 11019297 | 95% |
Reaction Steps
2940 g (30 mol) of cyclohexanone were heated to reflux while stirring and, at this temperature, a solution of 87.6 g (0.6 mol) of di-tert-butyl peroxide in 216 g (3 mol) of ethyl vinyl ether was added over the course of 5 hours (h). The mixture was subsequently refluxed for a further 1 h. After the mixture had cooled, the low boilers (tert-butanol, remaining vinyl ether and peroxide) and the excess cyclohexanone were removed by distillation under reduced pressure (25-40 mbar; diaphragm pump). The residue (about 500 g) was distilled under reduced pressure (0.5 to 2 mbar; oil pump). A total of 350 g of a 95% pure 2-(2-ethoxyethyl)cyclohexanone of boiling point 60°-65° C. (0.5 mbar) was obtained, corresponding to a yield of 69% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05489694 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-96ece210dd19420b8b8041f4b6f706f0 |
| Source note | uspto-grants-1996_02 |