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Boron trifluoride → 1-tert-Butyl-4-(3-chloro-2-methylpropyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Boron trifluoride | HCID 6356 | — |
| 反応物 | tert-BUTYL CHLORIDE | HCID 10486 | — |
| 反応物 | (3-Chloro-2-methylpropyl)benzene | HCID 13510156 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-tert-Butyl-4-(3-chloro-2-methylpropyl)benzene | HCID 13251817 | — |
| 生成物 | (3-Chloro-2-methylpropyl)benzene | HCID 13510156 | — |
反応手順
BF3 is passed for 30 minutes into a mixture of 84 parts by weight of 2-methyl-3-phenyl-propyl chloride and 50 ml of BF3 ·2H2O at room temperature. 56 parts by weight of tert.-butyl chloride are then added dropwise at room temperature. The mixture is refluxed for 4 hours and is then allowed to cool; the crude product is introduced into water and extracted with chloroform. The organic phase is separated off, washed with water, dried over Na2CO3 and distilled. 30 parts by weight of 2-methyl-3-phenyl-propyl chloride, boiling point 105° C./16 mm Hg, and 45 parts by weight of 2-methyl-3-(p-tert.-butylphenyl)-propyl chloride, boiling point 80° C.-81° C./0.02 mm Hg, are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04328380 |
| 出典データセット | uspto-grants-1982_05 |
| ORD ID | ord-62ed638def68417c87c569adbce2f41d |
| 出典メモ | uspto-grants-1982_05 |