HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanecarboxaldehyde → 1-Cyclohexyl-7-chloro-1-hepten-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | [(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chloride | HCID 73680070 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1-Cyclohexyl-7-chloro-1-hepten-3-one | HCID 57214934 | — |
Reaction Steps
2 parts of [(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chloride and 1.2 parts of cyclohexanecarbaldehyde were combined in 45 parts of xylene. This suspension was maintained under a nitrogen atmosphere and was refluxed for about 4 hours until a clear solution formed. After cooling the solution to room temperature, xylene was removed at a temperature of about 60° C. and under reduced pressure, leaving a product mixture. This mixture was separated chromatographically on a silica column using as the elution solvent 50 percent by volume of Skelly B in benzene, to yield 1-cyclohexyl-7-chloro-1-hepten-3-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04347192 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-192fe84647684fc38c7548455c798d5e |
| Source note | uspto-grants-1982_08 |