化工社化工社 化学情報印刷レポート · 研究参考用
Ammonium Chloride → Benzenemethanol, alpha-1-propen-1-yl-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Crotonaldehyde | HCID 447466 | — |
| 反応物 | HCID 178418255 | HCID 178418255 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Benzenemethanol, alpha-1-propen-1-yl- | HCID 219674 | 99.9% |
反応手順
To a cooled (0-55° C.) 927 mL of 1 M solution of phenyl magnesium bromide in tetrahydofuran was added dropwise a solution of crotonaldehyde (65.0 g) in 130 mL of anhydrous ether over a period of 2 hours and 45 minutes. The reaction was stirred for an additional 45 minutes and then warmed to room temperature. After four more hours of stirring, saturated ammonium chloride aqueous solution (750 mL) was added to the reaction. The mixture was extracted with 750 mL of ether twice. The combined extract was dried over anhydrous potassium carbonate and filtered. The solvent was evaporated to give 135.88 g (99.9%) of the desired 1-phenyl-2-buten-1-ol as an oil which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07902259B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-b3d8af6edac34ac28fd730ced29100ef |
| 出典メモ | uspto-grants-2011_03 |