HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917579Generated: November 2, 2026
Hydrochloric Acid → (3-Cyanophenylamino)-2-fluorophenylacetic acid
https://huagongshe.com/reaction/917579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromobenzonitrile | HCID 23381 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 2-Fluoro-DL-phenylglycine | HCID 580073 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | (3-Cyanophenylamino)-2-fluorophenylacetic acid | HCID 58962742 | — |
Reaction Steps
6.5 g (47.0 mmol) of potassium carbonate and 597 mg (3.10 mmol) of copper(l) iodide are added to a solution of 5.70 g (31.3 mmol) of 3-bromobenzonitrile and 5.30 g (31.3 mmol) of 2-fluoro-dl-alpha-phenylglycine in 30 ml of N,N-dimethylacetamide, and the mixture is stirred at 90° C. for 48 hours. The reaction mixture is then poured into 80 ml of 1N HCl and extracted twice with diethyl ether. The combined organic phases are extracted twice with 50 ml of 1N NaOH each time. The two basic aqueous phases are combined, acidified using 25% HCl and extracted twice with 80 ml of diethyl ether each time. These two organic phases are combined, dried using sodium sulfate and subsequently evaporated, giving (3-cyanophenylamino)-2-fluorophenylacetic acid as a yellowish solid; ESI 270.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07273867B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-d0e550f080fe4e90b59eb0eba4289ec8 |
|---|
| Source note | uspto-grants-2007_09 |
|---|