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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1910792생성일: 2026년 10월 25일

Tetrahydro-4H-pyran-4-ol → 2-Hydroxy-4-nitro-benzoic acid tetrahydro-pyran-4-yl ester

https://huagongshe.com/reaction/1910792

반응식

참여 물질

역할이름HCID투입량
반응물Tetrahydro-4H-pyran-4-olHCID 74956—
반응물2-Hydroxy-4-nitrobenzoyl chlorideHCID 12924720—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매TetrahydrofuranHCID 8028—
생성물2-Hydroxy-4-nitro-benzoic acid tetrahydro-pyran-4-yl esterHCID 6710639929.4%

반응 조건

온도45 °C

반응 단계

2-Hydroxy-4-nitro-benzoyl chloride (0.82 g, 4.07 mmol) in THF (15 mL) was added portionwise to a solution of 4-hydroxytetrahydropyran (0.8 mL, 8.1 mmol) in pyridine (4 μL) at 0° C., followed by a catalytic amount of 4-(dimethylamino)-pyridine (DMAP). The mixture was maintained overnight at 40-50° C. then diluted with water and extracted with ethyl acetate. The organic extract was washed successively with saturated sodium bicarbonate solution, water and brine solution, dried and concentrated to give a residue which was triturated with a mixture of DCM and petroleum ether. The residue was purified by flash column chromatography on silica, eluting with ethyl acetate/petroleum ether (2-15%) to give 2-hydroxy-4-nitro-benzoic acid tetrahydro-pyran-4-yl ester (0.32 g, 29%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604029B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-2441a56449c840ee8da829b3db925ebd
출처 메모uspto-grants-2013_12