HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | m-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcohol | HCID 54186887 | — |
| Product | 5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochloride | HCID 21510140 | — |
Reaction Steps
4 parts of m-chloro-α-(2-imidazolin-2-ylaminomethyl)benzyl alcohol are added portionwise to 20 parts of cooled (ice-bath) sulfuric acid solution 80%. Upon completion, the whole is stirred for 2 hours at room temperature. The reaction mixture is poured onto crushed ice and the whole is filtered over diatomaceous silica. The filtrate is alkalized with ammonium hydroxide solution at room temperature (cooling is necessary) and the product in base form is extracted with chloroform. The latter is dried and evaporated. The residue is converted into the hydrochloride salt in 2-propanol, yielding 5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochloride; m.p. 249.8°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03963718 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-276882242893435187dc3e52d8487aaf |
| Source note | uspto-grants-1976_06 |