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HRID 1708957作成日:2026年10月25日

1-Bromo-2-methylpropane → 2-(Benzylmethylamino)-3,7,11-trimethyl-3,7-dodecanediol

https://huagongshe.com/reaction/1708957

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-methylpropaneHCID 6555—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物4,8-Dimethyl-1-nonen-4-olHCID 19928733—
反応物3-(Phenethylamino)-butan-2-oneHCID 21786235—
反応物HCID 178418816HCID 178418816—
触媒Titanocene dichiorideHCID 124040768—
溶媒Diethyl EtherHCID 3283—
生成物2-(Benzylmethylamino)-3,7,11-trimethyl-3,7-dodecanediolHCID 1992874417%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04946857
出典データセットuspto-grants-1990_08
ORD IDord-66372e67de4849f8b999a37cb4631dcf
出典メモuspto-grants-1990_08