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HRID 604220作成日:2026年10月27日

Triisopropyl borate → 5-Carboxy-2-methoxybenzeneboronic acid

https://huagongshe.com/reaction/604220

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3-Bromo-4-methoxybenzoic acidHCID 66836—
反応物HCID 178418306HCID 178418306—
反応物HCID 178418348HCID 178418348—
溶媒Diethyl EtherHCID 3283—
溶媒PentaneHCID 8003—
溶媒TetrahydrofuranHCID 8028—
生成物5-Carboxy-2-methoxybenzeneboronic acidHCID 42614541—

反応条件

温度-78 °C

反応手順

3-Bromo-4-methoxybenzoic acid (2.00 g) is dissolved in tetrahydrofuran (50 ml), and the mixture is cooled to −78° C., and thereto is added dropwise a 1.1M methyllithium in diethyl ether (7.7 ml). The mixture is stirred at −78° C. for 5 minutes, and thereto is added dropwise a 1.6M tert-butyllithium in n-pentane (13.2 ml), and the mixture is stirred at −78° C. for 15 minutes, and the mixture is allowed to warm to −45° C., and the mixture is stirred for 45 minutes, and then again cooled to −78° C. Thereto is added dropwise triisopropylborate, and the mixture is stirred at −78° C. for 15 minutes, and the mixture is allowed to warm to room temperature. The mixture is stirred at room temperature for 1.5 hours, and the mixture is concentrated under reduced pressure, and thereto are added water and hexane. The aqueous layer is adjusted to pH 4 by addition of a 6N-hydrochloric acid and a saturated aqueous sodium bicarbonate solution, and the mixture is extracted with ethyl acetate and methanol twice. The organic layer is washed with a saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. To the resulting residue is added diethyl ether, and the resulting solids are collected by filtration to give 2-methoxy-5-carboxyphenylboronic acid (1.37 g) as a crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906517B2
出典データセットuspto-grants-2011_03
ORD IDord-fc068424a1c34518938f7da9c552d33d
出典メモuspto-grants-2011_03