돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223353생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/223353

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Nitrosylsulfuric acidHCID 82157—
반응물2,2-Dimethyl-7-nitro-2H-chromen-6-amineHCID 13222893—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
용매TolueneHCID 1140—
생성물2,2-dimethyl-6-iodo-7-nitro-2H-benzo[b]pyranHCID 1530770239.4%

반응 조건

온도8 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04353906
출처 데이터셋uspto-grants-1982_10
ORD IDord-6447c8afb02b4facb2a1934151259adf
출처 메모uspto-grants-1982_10