関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Bromo-2-methylpropane | HCID 6555 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | 4,8-Dimethyl-1-nonen-4-ol | HCID 19928733 | — |
| 反応物 | 3-(Phenethylamino)-butan-2-one | HCID 21786235 | — |
| 反応物 | HCID 178418816 | HCID 178418816 | — |
| 触媒 | Titanocene dichioride | HCID 124040768 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-(Benzylmethylamino)-3,7,11-trimethyl-3,7-dodecanediol | HCID 19928744 | 17% |
反応手順
To a solution of isobutylmagnesium bromide prepared from 14.6 g of magnesium, 68.5 g of isobutyl bromide and 500 ml of diethyl ether was added a solution of 34 g of 4,8-dimethyl-1-nonen-4-ol in 100 ml of diethyl ether dropwise under ice-cooling. After completion of the addition, 2.5 g of titanocene dichloride was added to the above solution at room temperature and the mixture was stirred at that temperature for 18 hours. Then, 38.2 g of 3-(benzylmethylamino)-2-butanone was added dropwise under ice-cooling and the mixture was stirred at that temperature for 30 minutes. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride and extracted with diethyl ether. The ether was distilled off, and after addition of chloroform, the residue was washed with a saturated aqueous solution of sodium chloride and a small amount of aqueous sodium hydrogen carbonate. After drying over anhydrous sodium sulfate, the chloroform was distilled off and the residue was subjected to silica gel column chromatography (elution with 95% methylene chloride-5% triethylamine) to give 11.3 g of 2-(benzylmethyl- amino)-3,7,11-trimethyl-3,7-dodecanediol [Compound (71)]. Yield 17%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04946857 |
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| 出典データセット | uspto-grants-1990_08 |
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| ORD ID | ord-66372e67de4849f8b999a37cb4631dcf |
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| 出典メモ | uspto-grants-1990_08 |
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