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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 706872생성일: 2026년 10월 25일

Hydrochloric Acid → 3-nitro-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamide

https://huagongshe.com/reaction/706872

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물(Oxan-4-yl)methanolHCID 2773573—
반응물4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-nitro-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamideHCID 67126458—

반응 단계

(Tetrahydro-2H-pyran-4-yl)methanol (2.0 g) in tetrahydrofuran (20 mL) was treated with 60% NaH (1.377 g). The solution was stirred for 20 minutes at the room temperature. To this solution was added 4-fluoro-3-nitrobenzenesulfonamide (2.84 g) portion-wise. The reaction was stirred for another 2 hours. The mixture was poured into water, neutralized with 10% HCl, and extracted with ethyl acetate three times. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified with flash column chromatography on silica gel eluting with 20-60% ethyl acetate in hexanes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09174982B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-4409d3be38a14b008ca3a4d5e3fed870
출처 메모uspto-grants-2015_11