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HRID 1712204作成日:2026年10月25日

Hydrochloric Acid → 3,5-Difluoro-4-(1-methylheptyloxy)phenylboronic acid

https://huagongshe.com/reaction/1712204

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Trimethyl borateHCID 8470—
反応物5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzeneHCID 68499982—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物3,5-Difluoro-4-(1-methylheptyloxy)phenylboronic acidHCID 68499248—

反応条件

温度-70 °C

反応手順

14.5 g of 1-bromo-3,5-difluoro-4-(1-methylheptyloxy)benzene from step 1 were dissolved in 150 ml of diethyl ether and cooled to −70° C. At this temperature, with cooling, firstly 31.0 ml of a 15% solution of butyllithium in n-hexane were slowly added dropwise, the mixture was stirred at the same temperature for 1 h, and then 5.6 ml of trimethyl borate were slowly added dropwise, and the mixture was stirred for a further h. The temperature of the reaction solution was slowly allowed to rise to −10° C. The mixture was then hydrolysed with distilled water, and the pH was adjusted to 2 using hydrochloric acid. The organic phase was separated off, and the aqueous phase was extracted with MTB ether. The product was subjected to conventional purification and dried over Na2SO4, giving 13.9 g of 3,5-difluoro-4-(1-methylheptyloxy)phenylboronic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790929B2
出典データセットuspto-grants-2010_09
ORD IDord-5af2f04a350c4adaabb2df1cab296330
出典メモuspto-grants-2010_09