HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → p-(1-Trifluoromethyl-heptyloxy)-benzamidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-(1-Trifluoromethyl-heptyloxy)-benzonitrile | HCID 15724839 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | p-(1-Trifluoromethyl-heptyloxy)-benzamidine hydrochloride | HCID 19097075 | — |
Reaction Steps
Into 20 ml of dry ethanol containing 3.76 g of oa p-(1-trifluoromethyl-heptyloxy)-benzonitrile, about 1 g of dry hydrogen chloride was introduced under stirring at a temperature below 10° C. After stirring at room temperature for 3 days, solvent was distilled off to obtain any oily product. To this, were added slowly 20 ml of dry ethanol containing about 2 g of ammonia under cooling with ice, followed by stirring at room temperature for 3 days. Ethanol and ammonia were removed to obtain 3.40 g of oily oa p-(1-trifluoromethyl-heptyloxy)-benzamidine hydrochloride. This oily hydrochloride was solidified by trituration in hexane to use the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05160662 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-7a17752d55cf424fb87d0eb350e298b4 |
| Source note | uspto-grants-1992_11 |