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HRID 341703作成日:2026年10月27日

Hydrochloric Acid → (4-Bromo-2,6-dimethylphenyl)boronic acid

https://huagongshe.com/reaction/341703

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-2-iodo-1,3-dimethylbenzeneHCID 2735573—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Bromo-2,6-dimethylphenyl)boronic acidHCID 5749730143.7%

反応条件

温度-75 °C

反応手順

To a solution of 4-bromo-2,6-dimethyl-1-iodobenzene (150 g, 0.48 mol) in tetrahydrofuran (1500 ml) at −75° C. is added n-butyl lithium (1.6 M in hexanes, 364 ml, 0.58 mol) dropwise maintaining the temperature of the reaction mixture below −70° C. When the addition is complete the mixture is stirred at −75° C. for an additional 30 minutes and then trimethyl borate (302 g, 2.9 mol) is added dropwise. After the addition is complete the reaction is stirred at −75° C. for 1 hour, then allowed to come to room temperature and stirred for 2 hours, followed by cooling in an ice bath and acidification with 0.5 N aqueous hydrochloric acid. The mixture is extracted with ethyl acetate (3×1000 ml) and the organic extracts are combined, washed with brine, dried over anhydrous sodium sulphate. The mixture is filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-bromo-2,6-dimethylphenylboronic acid (48 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895761B2
出典データセットuspto-grants-2014_11
ORD IDord-c6a1d681e830422eb8e2f8b1d14f81ac
出典メモuspto-grants-2014_11