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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288523Generated: November 3, 2026

Ethanol → HCID 21502441, compound

https://huagongshe.com/reaction/1288523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium IodideHCID 4875—
ReactantHCID 21502437HCID 21502437—
SolventWaterHCID 962—
ProductHCID 21502441HCID 2150244189.7%

Reaction Steps

A solution of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2-bromoethyl)ammonium bromide (1 g) and potassium iodide (0.54 g) in a mixed solvent of ethanol (5 cc) and water (5 cc) was stirred for 30 minutes at room temperature, and the reaction mixture was concentrated under reduced pressure. The residue was extracted with chloroform, and the solvent of the chloroform layer was distilled off. To the residue was added benzene, and the benzene layer was concentrated to dryness. The residue was recrystallized from a mixed solvent of acetonitrile and ether to give orange crystals (1.0 g) of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2-bromoethyl)ammonium iodide, m.p. 149°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03988373
Source datasetuspto-grants-1976_10
ORD IDord-337f62912a0c43f896a8bdaca1a6ecb8
Source noteuspto-grants-1976_10