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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223353Generated: October 25, 2026

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

https://huagongshe.com/reaction/223353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantNitrosylsulfuric acidHCID 82157—
Reactant2,2-Dimethyl-7-nitro-2H-chromen-6-amineHCID 13222893—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventTolueneHCID 1140—
Product2,2-dimethyl-6-iodo-7-nitro-2H-benzo[b]pyranHCID 1530770239.4%

Reaction Conditions

Temperature8 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04353906
Source datasetuspto-grants-1982_10
ORD IDord-6447c8afb02b4facb2a1934151259adf
Source noteuspto-grants-1982_10