関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | 1,5-Dibromopentane | HCID 8100 | — |
| 反応物 | Delta-Valerolactone | HCID 10953 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | 3,3-Dibromopentane | HCID 13555730 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(4'-Hydroxy-n-butyl)-1-cyclohexanol | HCID 15620769 | 73.6% |
反応手順
A solution of 1,5-dibromopentane (5 gms, 23.15 mmol) in dry THF (10 ml) was added slowly to a suspension of Magnesium turning (2.8 gms, 112 mmole) in dry THF (50 ml) and catalytic amount of iodine under nitrogen atmosphere. After the addition of about 3 ml of dibromopentane solution in THF, Grignard reaction was initiated. The addition was continued maintaining a gentle reflux. The mixture was refluxed for 16 hours to complete the formation of the Grignard reagent. To the reaction mixture was added a solution of a solution of δ-valerolactone (2.13 gms, 21.3 mmol) in dry THF (50 ml). The resulting mixture was refluxed for 6 hours under nitrogen and then quenched by addition of saturated solution of ammonium chloride at 0° C. The product was extracted in ethylacetate. Organic layer was washed with water, brine and dried over anh. Na2SO4. Drying agent was filtered off and the solvent was removed under vacuum to give 2.7 gms of diol (8), which was used without any further purification in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08097728B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-198eff842faa45ba93ef1839348a80c3 |
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| 出典メモ | uspto-grants-2012_01 |
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