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HRID 45407作成日:2026年10月24日

Potassium Nitrate → 4-(Ethylsulfonyl)-1-fluoro-2-nitrobenzene

https://huagongshe.com/ja/reaction/45407

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium NitrateHCID 24434—
反応物FluoresoneHCID 71814—
溶媒Sulfuric AcidHCID 1118—
生成物4-(Ethylsulfonyl)-1-fluoro-2-nitrobenzeneHCID 6736026366%

反応条件

温度90 °C

反応手順

To a solution of 1-(ethylsulfonyl)-4-fluorobenzene (1.36 mmol, 0.257 g) in sulfuric acid (1.32 ml) was added potassium nitrate (0.243 g) at 80° C. The mixture was stirred at 90° C. for 2 hours. Ice water (5 ml) was added and the mixture was extracted with ethyl acetate (25 ml) and washed with water (20 ml) and brine (10 ml). The organic extracts were combined and dried over sodium sulfate and concentrated. The residue was purified by column chromatography (hexane/ethylacetate 1:3) to give a light yellow solid which was crystallized from methanol. HPLC indicated 98% purity, mp 128-131° C., (0.21 g, 66% yield). 1H NMR (CDCl3): 1.35 (t, 3H, CH3), 3.21 (q, 2H, CH2), 7.55 (t, 1H, Ar—H), 8.21 (m, 1H, Ar—H), 8.64 (d, 1H, Ar—H); MS: 229 M−. Elemental Analysis (C, H, N, F, S) for C8H8FNO4S; calculated C, 41.20; H, 3.46; N, 6.01; F, 8.15; S, 13.75. found C, 41.31; H, 3.35; N, 5.85; F, 8.17; S, 13.53.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541476B2
出典データセットuspto-grants-2013_09
ORD IDord-f71feadad67f41ecaa39e431e9b6e979
出典メモuspto-grants-2013_09