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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985579Generated: October 30, 2026

Potassium Iodide → 2,3-Dihydro-4,7-dimethyl-5-[(2-methyl-2-propenyl)oxy]-1H-indole-1-carbaldehyde

https://huagongshe.com/reaction/985579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dihydro-5-hydroxy-4,7-dimethyl-1H-indole-1-carbaldehydeHCID 22506834—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2,3-Dihydro-4,7-dimethyl-5-[(2-methyl-2-propenyl)oxy]-1H-indole-1-carbaldehydeHCID 2250683682%

Reaction Conditions

Temperature80 °C

Reaction Steps

2,3-Dihydro-5-hydroxy-4,7-dimethyl-1H-indole-1-carbaldehyde (5.74 g, 30 mmol) was dissolved in N,N-dimethylformamide (100 ml) and to the solution were added potassium carbonate (8.29 g, 60 mmol), potassium iodide (0.50 g, 3 mmol) and 3-chloro-2-methyl-1-propene (4.41 ml, 45 mmol). The mixture was stirred at 80° C. for 3 hours. The reaction mixture was poured into cold water (300 ml), and extracted with ethyl acetate. The extract was washed with saturated brine and dried over sodium sulfate, and then the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel. (hexane:ethyl acetate=6:1) to obtain 6.00 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872718B1
Source datasetuspto-grants-2005_03
ORD IDord-889dec0651ec4b7ca502bb76c806e125
Source noteuspto-grants-2005_03