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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1059132생성일: 2026년 10월 27일

1,4-Dibromobenzene → 4-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]phenylboronic acid

https://huagongshe.com/reaction/1059132

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DibromobenzeneHCID 7804—
반응물Trimethyl borateHCID 8470—
반응물Ammonium ChlorideHCID 25517—
반응물isopropyl(1-trityl-1H-imidazol-4-yl)ketoneHCID 10150490—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물4-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]phenylboronic acidHCID 18668578—

반응 단계

To a solution of p-dibromobenzene (66.0 g) in THF (700 ml) was added dropwise a solution (1.6 M; 180 ml) of n-butyllithium in hexane at —78° C., and the mixture was stirred at the same temperature for 15 min. A solution of 2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanone (85.0 g) in THF (250 ml) was added dropwise, and the mixture was further stirred for 15 min. To the reaction mixture was added dropwise a solution (1.6 M; 270 ml) of n-butyllithium in hexane at −78° C., and the mixture was stirred at the same temperature for 15 min, which was followed by addition of trimethyl borate (196 ml). The reaction mixture was stirred at room temperature for 2 h, and an aqueous ammonium chloride solution was added. The mixture was stirred at room temperature for 12 h, and the organic layer was separated, washed with 1N sodium hydroxide and brine and dried over anhydrous magnesium sulfate. The solvent was evaporated to give a crude product (126 g) of the title compound as an amorphous powder. This product was used in a reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518257B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-f01ae4c47fd942f59dbb22b21f6a766f
출처 메모uspto-grants-2003_02