関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-one | HCID 162511 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol | HCID 21319801 | 106.5% |
反応手順
Into a 1 liter reaction flask equipped with a reflux condenser, thermometer, stirrer, dropping funnel and nitrogen inlet tube are placed 12 g (0.5 moles) of magnesium turnings and 250 cc anhydrous diethyl ether. Over a 2 hour period, 45.3 g (0.5 moles) of methallyl chloride is added. The Grignard solution is stirred for 1/2 hour and 28 g of 2-acetyl-3,3-dimethyl-5-norbornene is added over a 20 minute period. The mixture is stirred at reflux for 1/2 hour and then is hydrolyzed by the addition of saturated ammonium chloride solution. The organic layer is washed with water and dried over magnesium sulfate. The mixture is then filtered and the solvent evaporated to yield 40 g of an oil, which is then fractionated on a micro Vigreux column after adding thereto 5 g Primol® and a trace quantity of Ionox® .
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04120308 |
|---|
| 出典データセット | uspto-grants-1978_10 |
|---|
| ORD ID | ord-e6b2a754b2194a85a1b7f83fd1245ec9 |
|---|
| 出典メモ | uspto-grants-1978_10 |
|---|