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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604220생성일: 2026년 10월 27일

Triisopropyl borate → 5-Carboxy-2-methoxybenzeneboronic acid

https://huagongshe.com/reaction/604220

반응식

참여 물질

역할이름HCID투입량
반응물Triisopropyl borateHCID 21531—
반응물3-Bromo-4-methoxybenzoic acidHCID 66836—
반응물HCID 178418306HCID 178418306—
반응물HCID 178418348HCID 178418348—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물5-Carboxy-2-methoxybenzeneboronic acidHCID 42614541—

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906517B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-fc068424a1c34518938f7da9c552d33d
출처 메모uspto-grants-2011_03