Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288517Generated: November 3, 2026

2,4-Dichlorobenzyl chloride → [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2,4-dichlorobenzyl)ammonium chloride

https://huagongshe.com/reaction/1288517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
Reactant[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethylamineHCID 21502510—
SolventMethanolHCID 887—
Product[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2,4-dichlorobenzyl)ammonium chlorideHCID 21502536119.5%

Reaction Steps

A mixture of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethylamine (2.0 g), α,2,4-trichlorotoluene (3.0 g) and methanol (10 cc) was refluxed for 5 hours, and the solvent of the reaction mixture was distilled off under reduced pressure. The residue was dissolved in a small amount of benzene and thereto was added a large amount of ether. The precipitated oil was gathered by decantation and dissolved in a small amount of benzene and thereto was further added a large amount of ether. The solvent was distilled off to give colorless oil (4.5 g) of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2,4-dichlorobenzyl)ammonium chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03988373
Source datasetuspto-grants-1976_10
ORD IDord-09e3b92a5f514f1aa2ef29c21c8300f5
Source noteuspto-grants-1976_10