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HRID 223353作成日:2026年10月23日

Potassium Iodide → 2,2-dimethyl-6-iodo-7-nitro-2H-benzo[b]pyran

https://huagongshe.com/ja/reaction/223353

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Nitrosylsulfuric acidHCID 82157—
反応物2,2-Dimethyl-7-nitro-2H-chromen-6-amineHCID 13222893—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
溶媒TolueneHCID 1140—
生成物2,2-dimethyl-6-iodo-7-nitro-2H-benzo[b]pyranHCID 1530770239.4%

反応条件

温度8 °C

反応手順

To a cooled solution of 6-amino-2,2-dimethyl-7-nitro-2H-benzo[b]pyran (20.0 g)* in glacial acetic acid (800 ml) was added concentrated sulphuric acid (400 ml) and the solution stirred at 8° C. Nitrosyl sulphuric acid (prepared by dissolving sodium nitrite (6.62 g) in cold concentrated sulphuric acid (200 ml) the mixture being warmed to dissolved the solid then re-cooled to approximately 4° C.) was added keeping the temperature of the reaction mixture below 12° C. The dark, viscous mixture was stirred at approximately 7° C. for a further hour then poured into a cold (approximately 5° C.) solution of potassium iodide (15.27 g) in water (200 ml). Toluene (800 ml) was added to dissolve the resulting precipitate and the mixture stirred in an ice bath for 20 minutes, then at room temperature for 18 hours. The reaction mixture was diluted with water (500 ml), the organic phase was separated, washed with water, dried and evaporated in vacuo to afford the required 2,2-dimethyl-6-iodo-7-nitro-2H-benzo[b]pyran (11.84 g, 39%) as a red gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04353906
出典データセットuspto-grants-1982_10
ORD IDord-6447c8afb02b4facb2a1934151259adf
出典メモuspto-grants-1982_10