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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347849생성일: 2026년 10월 24일

Triisopropyl borate → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/ko/reaction/347849

반응식

참여 물질

역할이름HCID투입량
반응물Triisopropyl borateHCID 21531—
반응물Ammonium ChlorideHCID 25517—
반응물3,5-Dimethoxy(methoxymethyl)benzeneHCID 10329976—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 23080945—

반응 단계

To a solution of 3,5-dimethoxy(methoxymethyl)benzene (23.7 g) in tetrahydrofuran (500 mL) was added n-butyllithium (1.56M hexane solution; 100 mL) at −78° C., and the reaction mixture was stirred for 30 minutes while cooling with ice. After cooling the internal temperature of the obtained reaction mixture to −78° C., to a reaction mixture was added triisopropoxyborane (39 mL), and the internal temperature was raised to room temperature while stirring. After completion of the reaction, saturated aqueous ammonium chloride was added to the reaction mixture while cooling with ice, and then ethyl acetate was added to the reaction mixture, the organic extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (7.5 g) was obtained as a yellow oil from the ethyl acetate fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176216B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-a0ecb90d07af4a3f8329a3cbccacfce1
출처 메모uspto-grants-2007_02