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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721427Generated: November 3, 2026

Allyl iodide → HCID 22414898, compound

https://huagongshe.com/reaction/1721427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22414877HCID 22414877—
SolventDimethylformamideHCID 6228—
ProductHCID 22414898HCID 22414898—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 11.6 g (41.2 mmol) of 1-benzyl-2,3-dihydro-4-hydroxy-3,3,7-trimethyl-1H-indol-2-one and 8.6 g (62.2 mmol) of potassium carbonate in 120 ml of N,N-dimethylformamide was added 8.3 g (49.4 mmol) of allyl iodide, and the mixture was stirred overnight at 70° C. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed with water and dried. The solvent was evaporated and the residue was purified by column chromatography (silica gel, 7:1 mixture of n-hexane and ethyl acetate) to obtain 8.9 g (yield 67.2%) of colorless needles of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510366
Source datasetuspto-grants-1996_04
ORD IDord-db6f05847dab4bf09d63eb9f9d3c3873
Source noteuspto-grants-1996_04