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Cyclohexanecarboxaldehyde → 1-Cyclohexyl-7-chloro-1-hepten-3-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| 反応物 | [(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chloride | HCID 73680070 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 1-Cyclohexyl-7-chloro-1-hepten-3-one | HCID 57214934 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04347192 |
| 出典データセット | uspto-grants-1982_08 |
| ORD ID | ord-192fe84647684fc38c7548455c798d5e |
| 出典メモ | uspto-grants-1982_08 |