HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Chlorophenacyl bromide → 2-Amino-4-(4-chlorophenacyl)-1-(2-morpholinoethyl)benzimidazolium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | 1-(2-Morpholin-4-ylethyl)-2-aminobenzimidazole | HCID 568011 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Amino-4-(4-chlorophenacyl)-1-(2-morpholinoethyl)benzimidazolium bromide | HCID 67711814 | 95% |
Reaction Steps
A solution of 2.33 g (10 mmol) of 4-chlorophenacyl bromide in 25 ml of acetone is added to a hot solution of 2-amino-1-(2-morpholinoethyl)benzimidazole (2.46 g, 10 mmol) in 75 ml of acetone. The mixture is stirred, heated at the boil for 5 minutes and maintained at room temperature. Three hours later a precipitate of the title compound appears, which is filtered and washed with acetone and with ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05623073 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-aaf1ce63975b4e8fb7fd87ea52561c4b |
| Source note | uspto-grants-1997_04 |