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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656913Generated: October 29, 2026

Allyl iodide → 10-(2-Propen-1-yl)-2,3-dihydro[1,4]dioxino[2,3-h]quinolin-10-ium Iodide

https://huagongshe.com/reaction/656913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
Reactant2,3-Dihydro[1,4]dioxino[2,3-h]quinolineHCID 68996469—
SolventTolueneHCID 1140—
Product10-(2-Propen-1-yl)-2,3-dihydro[1,4]dioxino[2,3-h]quinolin-10-ium IodideHCID 6899119585.2%

Reaction Steps

2,3-Dihydro[1,4]dioxino[2,3-h]quinoline (3.65 g; 19.52 mmol) and allyl iodide (6.52 ml; 39.04 mmol) were refluxed in toluene (50 ml) at 100° C. After 2.5 h more allyl iodide (0.65 ml; 3.9 mmol) was added to the mixture and the reaction continued under the same conditions for a further 0.5 h. The solvent was removed and the tar like product washed with toluene. This was dried under high vacuum overnight to afford the desired product (5.91 g; 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-96f54fb39bca4ce888b0d6a92af84341
Source noteuspto-grants-2011_12