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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014179Generated: November 1, 2026

Acetone → HCID 67316339, compound

https://huagongshe.com/reaction/1014179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAllyl bromideHCID 7841—
ReactantHCID 21071594HCID 21071594—
ProductHCID 67316339HCID 6731633999%

Reaction Conditions

Temperature60 °C

Reaction Steps

To acetone (300 mL) was added 3-(3-methyl-4-nitrophenyl)pyridine (Intermediate B9, 20.25 g, 88.0 mmol)) and allyl bromide (42.6 g, 352.2 mmol, Aldrich), and the reaction was stirred at 60° C. for 12 h. Filtration removed the liquids and washing with MeOH (2×20 mL) afforded 3-[3-(methyloxy)-4-nitrophenyl]-1-(2-propen-1-yl)pyridinium bromide as a yellow solid (30.8 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-538c432c21694d398e92c90a7de8a549
Source noteuspto-grants-2011_07