戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 52622作成日:2026年10月25日

Triisopropyl borate → 5-Chloro-2-methoxyphenylboronic acid

https://huagongshe.com/reaction/52622

反応式

関与物質

役割名称HCID仕込み量
反応物Triisopropyl borateHCID 21531—
反応物2-Bromo-4-chloroanisoleHCID 521935—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-2-methoxyphenylboronic acidHCID 273575180.5%

反応条件

温度-70 °C

反応手順

A stirred solution of 5.8 grams (0.026 mole) of 3-bromo-4-methoxychlorobenzene in 150 mL of tetrahydrofuran was cooled to -80° C., and 11.5 mL of n-butyllithium in hexanes (2.5 Molar-0.029 mole) was added dropwise during a 15 minute period, while maintaining the reaction mixture temperature at about -70° C. The initial reaction was very exothermic, which required cooling the reaction mixture to about -100° C. Upon completion of the addition, the reaction mixture was stirred at -80° C. for 15 minutes. After this time, 17.5 mL (0.076 mole) triisopropyl borate was added during a 1 minute period. The reaction mixture was then allowed to warm slowly to ambient temperature during a 3 hour period, where it was stirred for an additional 1 hour. After this time, the reaction mixture was concentrated under reduced pressure to a volume of about 50 mL. The concentrate was then poured into 500 mL of ice-water. The mixture was then made acidic with about 26 mL of aqueous 2N hydrochloric acid. The mixture was then filtered to collect a solid, which was dried, yielding 3.9 grams of 5-chloro-2-methoxyphenylboronic acid. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616718
出典データセットuspto-grants-1997_04
ORD IDord-61f52a92539e4047b96dab6bf81b2d40
出典メモuspto-grants-1997_04