HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4-(trifluoromethyl)benzene-1-carboximidate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzonitrile, 4-(trifluoromethyl)- | HCID 67995 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 4-(trifluoromethyl)benzene-1-carboximidate hydrochloride | HCID 68765138 | 93% |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
A solution of 4-trifluoromethyl-benzonitrile (5.16 g, 30.2 mmol) and ethanol (1.39 ml, 30.2 mmol) in chloroform (15 ml) was saturated with a dry stream of HCl gas for 15 min. at −5° C. and the mixture allowed to stand 1 week at 4° C. The product was precipitated with ether, and the suspension stirred for 30 min. at −15°C., then filtered and washed with ether. The solid product was dried at r.t. under high vacuum overnight to afford the title compound (7.1 g, 28 mmol, 93% yield) as a white solid. MS: m/e=217 (M+), 172 (M+-EtOH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265426B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-7b3b0ce73772489aaab4a1dfbffeb6f5 |
| Source note | uspto-grants-2001_07 |