HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-chlorobenzimidate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzonitrile, m-chloro- | HCID 13015 | — |
| Product | Ethyl 3-chlorobenzimidate hydrochloride | HCID 21938143 | 100% |
Reaction Steps
To a solution of 3-chlorobenzonitrile (50 g, 363 mmol) in anhydrous ethanol (500 mL), cooled to 0° C. in an ice bath, was bubbled HCl (g) through a gas dispersion tube for approximately 20 minutes until the solution was saturated. The resulting reaction mixture was stirred at room temperature for 16 h. Volatiles were removed in vacuo and the residue was triturated with anhydrous ether (˜200 mL). The white solid was collected by filtration and dried in vacuo overnight to afford ethyl 3-chlorobenzimidate hydrochloride (INTERMEDIATE II.1) (80 g, 363 mmol, 100%) which was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820649B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-bb4e323615f34b59885f49acecccb010 |
| Source note | uspto-grants-2010_10 |