戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 993作成日:2026年10月23日

Hydrochloric Acid → (6-Methoxy-1-benzothiophen-2-yl)boronic acid

https://huagongshe.com/ja/reaction/993

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Triisopropyl borateHCID 21531—
反応物6-Methoxy-1-benzothiopheneHCID 13634237—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(6-Methoxy-1-benzothiophen-2-yl)boronic acidHCID 1056027671%

反応条件

温度0 °C

反応手順

To a solution of 6-methoxybenzo[b]thiophene (18.13 g, 0.111 mol) in 150 mL of anhydrous tetrahydrofuran (THF) at -60° C. was added n-butyllithium (76.2 mL, 0.122 mol, 1.6M solution in hexanes), dropwise via syringe. After stirring for 30 minutes, triisopropyl borate (28.2 mL, 0.122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then distributed between 1N hydrochloric acid and ethyl acetate (300 mL each). The layers were separated, and the organic layer was dried over sodium sulfate. Concentration in vacuo produced a white solid that was triturated from ethyl ether hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b]thiophene-2-boronic acid as a white solid. mp 200° C. (dec). 1H NMR (DMSO-d6) d 7.83 (s, 1H), 7.78 (d, J=8.6 Hz, 1H), 7.51 (d, J=2.0 Hz, 1H), 6.97 (dd, J=8.6, 2.0 Hz, 1H), 3.82 (s, 3H). FD mass spec: 208.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723474
出典データセットuspto-grants-1998_03
ORD IDord-b667ae6e1894401594ee757404717db3
出典メモuspto-grants-1998_03