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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium potassium tartrate tetrahydrate | HCID 2724148 | — |
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 반응물 | 6-Bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalene-2-carboxylic acid methyl ester | HCID 59326603 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [6-Bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalen-2-yl]-methanol | HCID 59326541 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642629B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-d4f90def062f47af9dd00947c8559b93 |
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| 출처 메모 | uspto-grants-2014_02 |
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