HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorine → Chloroadamantylidene adamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Biadamantylidene | HCID 141567 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Chloroadamantylidene adamantane | HCID 12950367 | — |
Reaction Steps
In Tetrahedron Letters 1970, 4579-82, J. H. Wieringa, J. Strating and H. Wynberg describe a process in which adamantylidene adamantane is reacted with chlorine is tetrachloromethane at a temperature of -20° to +10° C. to form 4-eq.-chloroadamantylidene adamantane in addition to polychlorinated products. The chloro-substituted adamantane compound is the starting point for further reaction in the presence of AgNO3 and THF/H2O to form a mixture of the corresponding 4-hydroxy-adamantylidene adamantane compounds, which with the appropriate oxidant (Jones reagent: CrO3, H2SO4, acetone) are finally converted into the corresponding ketone compound, in which the carbonyl group is in the 4-position.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705847 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-7546b11291c740d58d0e845bb8155701 |
| Source note | uspto-grants-1987_11 |