HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyltrimethylammonium hydroxide → HCID 70546733, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | N-(2,6-Dichlorophenyl)-N-(prop-2-yn-1-yl)-4,5-dihydro-1H-imidazol-2-amine | HCID 20332207 | — |
| Catalyst | Ethanol | HCID 702 | — |
| Product | HCID 70546733 | HCID 70546733 | 18.7% |
Reaction Steps
A mixture consisting of 5.4 gm of 2-[N-(2,6-dichloro-phenyl)-N-propargyl-amino]-2-imidazoline and 40 ml of ethanol containing 5 drops of trimethylbenzyl ammonium hydroxide was refluxed for five hours, while stirring. Thereafter, the ethanol was evaporated in vacuo, and the residue was dissolved in dilute hydrochloric acid. The resulting solution was fractionally extracted with ether at stepwisely increasing pH-values (addition of 2 N sodium hydroxide). The thin-layer chromatographically uniform ethereal fractions having a pH of 9 or more were combined, dried over magnesium sulfate, and the ether was evaporated in vacuo, leaving 1 gm (18.7% of theory) of 7-(2,6-dichloro-phenyl)-2,3-dihydro-5-methyl-imidazo[1,2-α]imidazole, m.p. 113°-117° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04210659 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-03058b514d05496faa348475546a3566 |
| Source note | uspto-grants-1980_07 |