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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238634생성일: 2026년 10월 25일

Sodium potassium tartrate tetrahydrate → [6-Bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalen-2-yl]-methanol

https://huagongshe.com/reaction/238634

반응식

참여 물질

역할이름HCID투입량
반응물Sodium potassium tartrate tetrahydrateHCID 2724148—
반응물DiisobutylaluminumhydrideHCID 21225700—
반응물6-Bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalene-2-carboxylic acid methyl esterHCID 59326603—
용매TetrahydrofuranHCID 8028—
생성물[6-Bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalen-2-yl]-methanolHCID 5932654199%

반응 단계

To a solution of 6-bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalene-2-carboxylic acid methyl ester (280 mg, 0.63 mmol) in tetrahydrofuran (5 mL) was added a solution of diisobutylaluminum hydride (1 M in toluene, 1.3 mL, 1.3 mmol) dropwise at −78° C. under a nitrogen atmosphere. The resulting mixture was warmed to room temperature and stirred at room temperature (the total stirring time between −78° C. and room temperature was 3 hours). The reaction mixture was treated with an aqueous solution of potassium sodium tartrate tetrahydrate at 0° C., warmed to room temperature, and stirred at room temperature for 30 min. The resulting mixture was extracted with ethyl acetate (20 mL×3). The combined organic layers were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel chromatography (silica gel, 100-200 mesh, 30% ethyl acetate in petroleum ether) to give [6-bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalen-2-yl]-methanol (263 mg, 99%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642629B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d4f90def062f47af9dd00947c8559b93
출처 메모uspto-grants-2014_02