HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-(2-Dimethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 2-(Bromomethyl)-N,N-dimethylaniline hydrobromide | HCID 19847386 | — |
| Reactant | HCID 178527818 | HCID 178527818 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-(2-Dimethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole | HCID 14181145 | — |
Reaction Steps
2.9 g of 2-dimethylaminobenzyl bromide hydrobromide are added to a solution of 1.56 g of 2-mercaptothieno[3,4-d]imidazole in 20 ml of anhydrous dimethylacetamide. A crystalline precipitate separates out in a weakly exothermic reaction. The mixture is stirred at room temperature for one hour, acetone is added, and the crystals are filtered off and dried in a stream of air. The crystalline solid is then introduced into saturated aqueous NaHCO3 solution, the mixture is heated briefly on a steam bath and, after stirring at room temperature, the crystals are filtered off. Treatment with active charcoal in ethanol and concentration is followed by solution being induced to crystallize with a little acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871734 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-a59278121bbd4263910513c12f79cb59 |
| Source note | uspto-grants-1989_10 |