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Chlorine → Chloroadamantylidene adamantane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chlorine | HCID 24526 | — |
| 反応物 | Biadamantylidene | HCID 141567 | — |
| 溶媒 | Carbon Tetrachloride | HCID 5943 | — |
| 生成物 | Chloroadamantylidene adamantane | HCID 12950367 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04705847 |
| 出典データセット | uspto-grants-1987_11 |
| ORD ID | ord-7546b11291c740d58d0e845bb8155701 |
| 出典メモ | uspto-grants-1987_11 |