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HRID 347869作成日:2026年10月27日

Trimethyl borate → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/reaction/347869

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl borateHCID 8470—
反応物Ammonium ChlorideHCID 25517—
反応物2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 23080945—

反応条件

温度-10 °C

反応手順

n-Butyllithium (2.64M hexane solution; 182 mL) was added dropwise to a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (121.3 g) in tetrahydrofuran (730 mL) at −78° C., and the mixture was stirred for 20 minutes. A solution of trimethoxyborane (61.7 mL) in tetrahydrofuran (20 mL) was then added to the reaction mixture at −78° C. When internal temperature was raised to −10° C., to the reaction mixture was added saturated aqueous ammonium chloride (730 mL), and stirring was continued for 15 minutes. The obtained reaction mixture was extracted with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (90.4 g) was obtained as a white solid from the n-hexane:ethyl acetate (2:3) fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176216B2
出典データセットuspto-grants-2007_02
ORD IDord-98cd5e7682ec4cf5b59bbbfda0652f27
出典メモuspto-grants-2007_02