HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylaminobenzyl bromide hydrobromide → 2-(2-Ethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylaminobenzyl bromide hydrobromide | HCID 19847389 | — |
| Reactant | HCID 178527818 | HCID 178527818 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Ethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole | HCID 14181149 | — |
Reaction Steps
1.12 g of 2-ethylaminobenzyl bromide hydrobromide are added to a solution of 0.60 g of 2-mercaptothieno-[3,4-d]imidazole in 100 ml of acetone. After the mixture has been stirred at room temperature for 24 hours, the solvent is removed by distillation in vacuo, and the crystalline residue is washed with acetone. Then 1N NH4OH solution is added to the product, the mixture is stirred for 2 hours, and the solid is filtered off with suction and washed wit water. The residue which has been dried in air is dissolved in methylene chloride, active charcoal is added, and the mixture is filtered. Concentration in vacuo results in the clorless crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871734 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-c3da992faa2e434ca5fd5483bc36f024 |
| Source note | uspto-grants-1989_10 |