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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614352Generated: October 29, 2026

Allyl bromide → HCID 21329311, compound

https://huagongshe.com/reaction/614352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 54270804HCID 54270804—
SolventAcetoneHCID 180—
ProductHCID 21329311HCID 21329311—

Reaction Steps

To a stirred suspension of 4.6 g. (0.016 mole) of the imidazopyridine product of Step C in 175 ml. of acetone, was added 1.8 g. (0.032 mole) of powdered potassium hydroxide. After stirring at room temperature for 20 minutes, 3.9 g. (0.032 mole) of allylbromide was added. Stirring at room temperature was continued overnight and the mixture then was concentrated to one-half volume. The concentrate was diluted with 150 ml. of water and the crude product was collected by filtration. The crude product was crystallized from 70 ml. of ethanol giving 2.0 g. of needles melting at 146°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04144341
Source datasetuspto-grants-1979_03
ORD IDord-e4699a2cc75d4c08b7f97b5e8bab0889
Source noteuspto-grants-1979_03