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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425370Generated: October 28, 2026

Potassium Iodide → N-Benzyl-6,6-dimethyl-1H-pyrano[2,3-f]indole-2,3-dione

https://huagongshe.com/reaction/2425370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
ReactantN-Benzyl-5-hydroxyisatinHCID 59134289—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
ProductN-Benzyl-6,6-dimethyl-1H-pyrano[2,3-f]indole-2,3-dioneHCID 591343328%

Reaction Conditions

Temperature200 °C

Reaction Steps

Under nitrogen stream, a solution of N-benzyl-5-hydroxyisatin (4.74 g, 18.7 mmol), potassium iodide (5.09 g, 31.8 mmol), potassium carbonate (5.17 g, 37.4 mmol), copper iodide (71 mg, 0.37 mmol) and 3-chloro-3-methyl-1-butyne (4.83 mL, 43.0 mmol) in DMF (47 mL) was stirred at 70° C. for 2 hours. Upon the completion of the reaction, saturated ammonium chloride aqueous solution was added thereto, the resulting solution was extracted with ethyl acetate. The resulting organic phase was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, concentrated and purified by silica gel short column (chloroform). 1,2-Dichlorobenzene (9 mL) was added and the resulting mixture was stirred at 200° C. for 30 minutes. After concentrating the reaction solution, the residue was purified by silica gel column (hexane/ethyl acetate=5/1) to obtain the aimed product (yield: 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964623B2
Source datasetuspto-grants-2011_06
ORD IDord-325fdad345cf498d815f53c290d6fe5b
Source noteuspto-grants-2011_06