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HRID 583645作成日:2026年10月26日

Trimethyl borate → 4-(tert-Butyldimethylsilyloxy)phenylboronic Acid (contains varying amounts of Anhydride)

https://huagongshe.com/reaction/583645

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BorateHCID 26574—
反応物(4-Bromophenoxy)(tert-butyl)dimethylsilaneHCID 4227167—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-(tert-Butyldimethylsilyloxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 1110781587.2%

反応条件

温度-70 °C

反応手順

A dry reactor equipped with two addition funnels, nitrogen inlet, and a mechanical stirrer was set up over a dry ice bath. To one of the addition funnels was added a filtered, preformed Grignard reagent from the reaction of 4-(t-butyldimethylsilyloxy)-bromobenzene (28.7 g, 0.1 mol) with magnesium turnings (2.96 g, 0.12 mol) in THF (70 mL). To the other addition funnel was added trimethylborate (12.48 g, 0.12 mol) in THF (50 mL). The reactor was charged with about 10 mL of the borate solution and was cooled to -70° C. About 10 mL of the Grignard solution was then added. The remaining borate and Grignard solutions were then added in aliquots in such a way as to ensure a slight excess of borate. The reaction mixture was stirred at -70° C. for one hour then stirred at room temperature for 20 hours. The reactor was cooled to 0° C. and water (100 mL) was slowly added with vigorous stirring. The mixture was extracted with ether (400 mL). The ether layer was washed with water (2×200 mL), dried over anhydrous MgSO4, then concentrated on a roto-evaporator to afford a light-tan-colored solid (22.0 g, 87 percent). 1H and 13C NMR spectra were consistent with the following structure. ##STR11##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929194
出典データセットuspto-grants-1999_07
ORD IDord-e6190e10235b4323be72aaeca7eb53ab
出典メモuspto-grants-1999_07