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HRID 341697作成日:2026年10月25日

Hydrochloric Acid → 4-Bromo-2-ethylphenylboronic acid

https://huagongshe.com/reaction/341697

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4-Bromo-2-ethyl-1-iodobenzeneHCID 2761396—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4-Bromo-2-ethylphenylboronic acidHCID 5927601745.4%

反応条件

温度-75 °C

反応手順

To a solution of 4-bromo-2-ethyl-1-iodobenzene (80 g, 0.25 mol) in tetrahydrofuran (800 ml) at −75° C. is added n-butyl lithium (1.6 M in hexanes, 188 ml, 0.3 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 (153.7 g, 1.48 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 (3×500 ml) and the organic fractions are combined, washed with brine, then 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-ethylphenylboronic acid (26 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-e37ad10e6fd743f19548917ccae87efc
出典メモuspto-grants-2014_11