化工社化工社 化学情報印刷レポート · 研究参考用
Ammonium Chloride → (6R)-2,6-Dimethylnon-2-ene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 反応物 | (S)-(+)-Citronellyl bromide | HCID 10900106 | — |
| 反応物 | HCID 178418332 | HCID 178418332 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (6R)-2,6-Dimethylnon-2-ene | HCID 15345839 | — |
反応手順
To (S)-citronellyl bromide (50 g, 0.228 mol) in THF (800 mL) at 0° C. was added LiCl (4.3 g) followed by CuCl2 (6.8 g). After 30 minutes methylmagnesium chloride (152 mL of a 3 M solution in THF, Aldrich) was added and the solution warmed to room temperature. After 10 hours the solution was cooled to 0° C. and a saturated aqueous solution of ammonium chloride carefully added. The resultant two layers were separated and the aqueous phase extracted with ether. The combined organic phases were dried (MgSO4) and concentrated to give an oil. 32.6 g; 93%. Used without further purification. 13C. NMR (100 MHz; CDCl3) 131.13, 125.28, 39.50, 37.35, 32.35, 25.92, 25.77, 20.31, 19.74, 17.81, 14.60.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07189747B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-88e7adfd224d4b419500f17402ab1401 |
| 出典メモ | uspto-grants-2007_03 |