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HRID 706872作成日:2026年10月26日

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

https://huagongshe.com/reaction/706872

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物(Oxan-4-yl)methanolHCID 2773573—
反応物4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-nitro-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamideHCID 67126458—

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09174982B2
出典データセットuspto-grants-2015_11
ORD IDord-4409d3be38a14b008ca3a4d5e3fed870
出典メモuspto-grants-2015_11