戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 264597作成日:2026年10月26日

Hydrochloric Acid → 4'-Pentyloxybiphenyl-4-boronic Acid

https://huagongshe.com/reaction/264597

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4-Bromo-4'-(pentyloxy)-1,1'-biphenylHCID 2801388—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4'-Pentyloxybiphenyl-4-boronic AcidHCID 1135807184.3%

反応条件

温度-78 °C

反応手順

To a stirred suspension of 4-(4-n-pentoxyphenyl)bromobenzene (1.0 g, 3.13 mmol) in anhydrous tetrahydrofuran (20 ml) at -78° C. under a nitrogen atmosphere was added n-butyllithium in hexanes (2.5M, 1.32 ml, 3.30 mmol). After a period of 15 rain, triisopropylborate (760 μl, 3.30 mmol) was added. Stirring at -78° C. was continued for 15 min and then at 25° C. for 40 min. The mixture was acidified with 0.5N HCl (20 mL) and then partitioned between ether (50 ml) and water (40 ml). The organic phase was washed with water (3×) and brine and dried with magnesium sulfate. The solvent was removed in vacuo to give 4-(4-n-pentoxyphenyl)phenylboronic acid (750 mg) as a solid: 1H NMR (400 MHz, DMSO-d6) δ0.89 (t, 3H, J=7.2 Hz), 1.38 (m, 4H), 1.72 (m, 2H), 3.99 (t, 2H, 1-6.5Hz), 6.99 (d, 2H, J=8.8 Hz), 7.57 (d, 2H, J=8.2 Hz), 7.60 (d, 2H, J=8.8 Hz), 7.83 (d, 2H, J=8.2 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646245
出典データセットuspto-grants-1997_07
ORD IDord-795bc943dcb3460594dfe3d775cf1ec5
出典メモuspto-grants-1997_07