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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872477Generated: November 2, 2026

Allyl bromide → HCID 11521507, compound

https://huagongshe.com/reaction/1872477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantDiethylamineHCID 8021—
Reactant2-Propen-1-amine, N,N-diethyl-HCID 79748—
ReactantHCID 131721961HCID 131721961—
SolventAcetoneHCID 180—
ProductHCID 11521507HCID 11521507—

Reaction Steps

The diethyidiallylammonium bromide monomer was prepared in two steps. 60.5 Grams (0.5 mol) of allyl bromide were slowly added to 160 grams (2.20 mol) of diethylamine in 100 milliliters of acetone. After about 15 minutes, the solution became cloudy and white crystals of the byproduct, allyl ammonium hydrogen bromide, were formed. The solution containing allyldiethyl amine was filtered, and distilled at 112° C. under nitrogen to purify the material. The allyldiethyl amine was redissolved in 200 milliliters of acetone, and more allyl bromide added slowly. Crystals of the product, diallydiethylammonium bromide, precipitated out immediately. The product was recovered by filtration and washed with several quantities of acetone, and dried under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110636
Source datasetuspto-grants-2000_08
ORD IDord-5519be56567f460a895a8b94182e346a
Source noteuspto-grants-2000_08