HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzyl chloride → [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2,4-dichlorobenzyl)ammonium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethylamine | HCID 21502510 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(2,4-dichlorobenzyl)ammonium chloride | HCID 21502536 | 119.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03988373 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-09e3b92a5f514f1aa2ef29c21c8300f5 |
| Source note | uspto-grants-1976_10 |