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HRID 617274作成日:2026年10月26日

1,6-Dibromohexane → 12-Bromo-3-methyl-6-oxadodecan-1-ol

https://huagongshe.com/reaction/617274

反応式

関与物質

役割名称HCID仕込み量
反応物1,6-DibromohexaneHCID 12368—
反応物3-Methyl-1,5-pentanediolHCID 20524—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物12-Bromo-3-methyl-6-oxadodecan-1-olHCID 1106586065.1%

反応手順

118 g (1.0 mol) of 3-methyl-1,5-pentanediol and 317 g (1.3 mol) of 1,6-di-bromohexane in 2.5 l of dioxan were treated at room temperature with 28 g (1.1 mol) of 95 percent sodium hydride and subsequently heated under reflux for 24 h. After cooling the reaction mixture was treated with 400 ml of water, neutralized with saturated ammonium chloride solution and subsequently extracted three times with 1 l of tert-butyl methyl ether each time. The combined organic extracts were washed with saturated ammonium chloride solution, dried over magnesium sulphate and concentrated on a rotary evaporator. Starting material and byproducts were removed by distillation in a vacuum at 150° C. bath temperature and 0.09 mbar. As the distillation residue there were obtained 183 g of 66 percent 12-bromo-3-methyl-6-oxadodecan-1-ol (43%), which is sufficiently pure for the further reactions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05948812
出典データセットuspto-grants-1999_09
ORD IDord-61bebb9fccbc45e99a9e77bd6691e0eb
出典メモuspto-grants-1999_09