関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 反応物 | Nerol | HCID 643820 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Neryl chloride | HCID 5874259 | 85% |
反応手順
To a stirred solution of 10.0 g (64.83 mmol) of (Z)-3,7-dimethyl-2,6-octadien-1-ol and 9.42 mL (71.31 mmol) of 2,4,6-collidine under argon at room temperature was added dropwise 2.74 g (64.83 mmol) of lithium chloride in 30 mL of DMF. The mixture was cooled to 0° C. and treated with 5.52 mL (71.31 mmol) of methanesulfonyl chloride dropwise over 10 minutes. The reaction was stirred at 0° C. for 4 hours (solid present), then was poured into 300 mL of ice/water. The aqueous solution was washed three times with 200 mL portions of hexane. The organic layers were combined and washed with 5% KHSO4, water, saturated NaHCO3, brine, dried (MgSO4) and evaporated to provide 9.48 g (85%) of title chloride as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05157027 |
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| 出典データセット | uspto-grants-1992_10 |
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| ORD ID | ord-b1564ab221984964bfcee046024bb453 |
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| 出典メモ | uspto-grants-1992_10 |
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