HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → rac. N-allyl-1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine | HCID 13324057 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | rac. N-allyl-1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine | HCID 13324058 | — |
Reaction Steps
4.9 g of 1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine are dissolved in 50 ml of acetone. Thereupon, 3.5 g of potassium carbonate are added, 1.8 ml of allyl bromide are slowly added dropwise while stirring, and the mixture is stirred overnight. Subsequently, the precipitate is removed by filtration, and the filtrate is evaporated, and rac. N-allyl-1-(m-methoxyphenyl)-N-methyl-2-cyclohexene-1-ethylamine remains as the residue. The hydrochloride of this compound melts at 114°-116° C. (after recrystallization from ethyl acetate/diisopropyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336268 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-1d5e6365ae9a488b9ecfafcb544012c5 |
| Source note | uspto-grants-1982_06 |