関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | tert-Butyl peroxybenzoate | HCID 11966 | — |
| 反応物 | 4-Chloro-alpha-methylstyrene | HCID 74381 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | 4,4'-Diisopropenylbiphenyl | HCID 13422373 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | P-tert-Butoxy-alpha-methyl styrene | HCID 11206291 | 69.3% |
反応手順
The procedure of Example 1 was repeated, except that there was utilized 16.9 grams (0.70 mole) of magnesium metal and 100 grams (0.66 mole) of 4-chloro-α-methylstyrene dissolved in 200 ml. of tetrahydrofuran. The Grignard reaction was started by the addition of a small amount of methyl iodide. After the reaction mixture had been refluxed for 12 hours, there was added at 0° C. in a dropwise manner a solution of 85 grams of t-butylperbenzoate in 300 ml. of ethylether. A crystalline product identified as 4,4'-diisopropenylbiphenyl was isolated from the oil which was recovered by filtering the mixture and washing with methanol. After stripping the methanol, a 69.3% yield of 4-t-butoxy-α-methylstyrene was isolated by fractional distillation as a colorless liquid having a boiling point of 65°-68° C. at 0.03 millimeters.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04603101 |
|---|
| 出典データセット | uspto-grants-1986_07 |
|---|
| ORD ID | ord-63997216ebee447ba405a25cc1993547 |
|---|
| 出典メモ | uspto-grants-1986_07 |
|---|